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Tomas Hudlicky, Ph.D. - Publications

Affiliations: 
1978-1982 Illinois Institute of Technology, Chicago, IL, United States 
 1982-1995 Virginia Polytechnic Institute and State University, Blacksburg, VA, United States 
 1995-2003 University of Florida, Gainesville, Gainesville, FL, United States 
 2003-2022 Brock University, Saint Catharines, Ontario, Canada 
Area:
synthetic organic chemistry
Website:
http://www.brocku.ca/tomas-hudlicky
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Year Citation  Score
2022 Habaz L, Bedard K, Smith M, Du L, Kornienko A, Hudlicky T. Design and Synthesis of C-1 Methoxycarbonyl Derivative of Narciclasine and Its Biological Activity. Molecules (Basel, Switzerland). 27. PMID 35744934 DOI: 10.3390/molecules27123809  0.358
2021 Ticli V, Zhao Z, Du L, Kornienko A, Hudlicky T. Synthesis and biological evaluation of 10-benzyloxy-Narciclasine. Tetrahedron. 101. PMID 35058668 DOI: 10.1016/j.tet.2021.132505  0.357
2021 Wicks C, Hudlicky T, Rinner U. Morphine alkaloids: History, biology, and synthesis. The Alkaloids. Chemistry and Biology. 86: 145-342. PMID 34565506 DOI: 10.1016/bs.alkal.2021.04.001  0.681
2019 Endoma-Arias MA, Dela Paz H, Hudlicky T. Chemoenzymatic Total Synthesis of (+)-10-Keto-Oxycodone from Phenethyl Acetate. Molecules (Basel, Switzerland). 24. PMID 31557873 DOI: 10.3390/Molecules24193477  0.474
2019 Makarova M, Endoma-Arias MA, Dela Paz H, Simionescu R, Hudlicky T. Chemoenzymatic total synthesis of ent-oxycodone: Second, third and fourth generation strategies. Journal of the American Chemical Society. PMID 31184866 DOI: 10.1021/Jacs.9B05033  0.408
2019 Makarova M, Rycek L, Hajicek J, Baidilov D, Hudlicky T. Tetrodotoxin: History, Biology, and Synthesis. Angewandte Chemie (International Ed. in English). PMID 30856678 DOI: 10.1002/Anie.201901564  0.796
2019 Baidilov D, Miskey S, Hudlicky T. Rapid Access to the Tricyclic Core of Calyciphylline A -Type Alkaloids Through Allyl Cyanate-to-Isocyanate Rearrangement European Journal of Organic Chemistry. 2019: 7590-7595. DOI: 10.1002/Ejoc.201901549  0.307
2018 Borra S, Lapinskaite R, Kempthorne C, Liscombe D, McNulty J, Hudlicky T. Isolation, Synthesis, and Semisynthesis of Amaryllidaceae Constituents from Narcissus and Galanthus sp.: De Novo Total Synthesis of 2- epi-Narciclasine. Journal of Natural Products. PMID 29787267 DOI: 10.1021/Acs.Jnatprod.8B00218  0.421
2018 Baidilov D, Rycek L, Trant JF, Froese J, Murphy B, Hudlicky T. Chemoenzymatic Approach to Tetrodotoxin: Synthesis of Fukuyama's, Alonso's, and Sato's Advanced Intermediates. Angewandte Chemie (International Ed. in English). PMID 29750851 DOI: 10.1002/Anie.201804602  0.804
2018 Endoma-Arias MA, Makarova M, Dela Paz H, Hudlicky T. Chemoenzymatic Total Synthesis of (+)-Oxycodone from Phenethyl Acetate Synthesis. 51: 225-232. DOI: 10.1055/s-0037-1611335  0.383
2018 Endoma-Arias MA, Makarova M, Dela Paz H, Hudlicky T. Chemoenzymatic Total Synthesis of (+)-Oxycodone from Phenethyl Acetate Synthesis. 51: 225-232. DOI: 10.1055/s-0037-1611335  0.383
2018 Endoma-Arias MA, Makarova M, Dela Paz H, Hudlicky T. Chemoenzymatic Total Synthesis of (+)-Oxycodone from Phenethyl Acetate Synthesis. 51: 225-232. DOI: 10.1055/s-0037-1611335  0.383
2018 Endoma-Arias MA, Makarova M, Dela Paz H, Hudlicky T. Chemoenzymatic Total Synthesis of (+)-Oxycodone from Phenethyl Acetate Synthesis. 51: 225-232. DOI: 10.1055/S-0037-1611335  0.383
2018 Endoma-Arias MA, Makarova M, Dela Paz H, Hudlicky T. Chemoenzymatic Total Synthesis of (+)-Oxycodone from Phenethyl Acetate Synthesis. 51: 225-232. DOI: 10.1055/s-0037-1611335  0.383
2018 Endoma-Arias MA, Makarova M, Dela Paz H, Hudlicky T. Chemoenzymatic Total Synthesis of (+)-Oxycodone from Phenethyl Acetate Synthesis. 51: 225-232. DOI: 10.1055/S-0037-1611335  0.383
2018 Hudlicky T, Baidilov D, Makarova M, Rycek L. Preparation of Rearranged Allylic Isocyanates from the Reaction of Allylic Alcohols with 1-Cyano-4-dimethylaminopyridinium Bromide Synthesis. 50: 4606-4610. DOI: 10.1055/S-0037-1610659  0.34
2018 Ryan W, Bedard K, Baidilov D, Tius M, Hudlicky T. Repetition of chemistry from a recently retracted paper. A cautionary note Tetrahedron Letters. 59: 2467-2469. DOI: 10.1016/J.Tetlet.2018.05.042  0.334
2018 Baidilov D, Rycek L, Trant JF, Froese J, Murphy B, Hudlicky T. Inside Back Cover: Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin (Angew. Chem. Int. Ed. 34/2018) Angewandte Chemie International Edition. 57: 11079-11079. DOI: 10.1002/Anie.201806823  0.712
2018 Baidilov D, Rycek L, Trant JF, Froese J, Murphy B, Hudlicky T. Inside Back Cover: Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin (Angew. Chem. Int. Ed. 34/2018) Angewandte Chemie International Edition. 57: 11079-11079. DOI: 10.1002/anie.201806823  0.349
2018 Baidilov D, Rycek L, Trant JF, Froese J, Murphy B, Hudlicky T. Inside Back Cover: Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin (Angew. Chem. Int. Ed. 34/2018) Angewandte Chemie International Edition. 57: 11079-11079. DOI: 10.1002/anie.201806823  0.349
2018 Baidilov D, Rycek L, Trant JF, Froese J, Murphy B, Hudlicky T. Inside Back Cover: Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin (Angew. Chem. Int. Ed. 34/2018) Angewandte Chemie International Edition. 57: 11079-11079. DOI: 10.1002/anie.201806823  0.349
2018 Baidilov D, Rycek L, Trant JF, Froese J, Murphy B, Hudlicky T. Inside Back Cover: Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin (Angew. Chem. Int. Ed. 34/2018) Angewandte Chemie International Edition. 57: 11079-11079. DOI: 10.1002/anie.201806823  0.349
2018 Baidilov D, Rycek L, Trant JF, Froese J, Murphy B, Hudlicky T. Inside Back Cover: Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin (Angew. Chem. Int. Ed. 34/2018) Angewandte Chemie International Edition. 57: 11079-11079. DOI: 10.1002/anie.201806823  0.349
2018 Baidilov D, Rycek L, Trant JF, Froese J, Murphy B, Hudlicky T. Inside Back Cover: Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin (Angew. Chem. Int. Ed. 34/2018) Angewandte Chemie International Edition. 57: 11079-11079. DOI: 10.1002/anie.201806823  0.349
2018 Baidilov D, Rycek L, Trant JF, Froese J, Murphy B, Hudlicky T. Inside Back Cover: Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin (Angew. Chem. Int. Ed. 34/2018) Angewandte Chemie International Edition. 57: 11079-11079. DOI: 10.1002/anie.201806823  0.349
2018 Baidilov D, Rycek L, Trant JF, Froese J, Murphy B, Hudlicky T. Innenrücktitelbild: Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin (Angew. Chem. 34/2018) Angewandte Chemie. 130: 11247-11247. DOI: 10.1002/Ange.201806823  0.731
2018 Baidilov D, Rycek L, Trant JF, Froese J, Murphy B, Hudlicky T. Innenrücktitelbild: Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin (Angew. Chem. 34/2018) Angewandte Chemie. 130: 11247-11247. DOI: 10.1002/ange.201806823  0.392
2018 Baidilov D, Rycek L, Trant JF, Froese J, Murphy B, Hudlicky T. Innenrücktitelbild: Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin (Angew. Chem. 34/2018) Angewandte Chemie. 130: 11247-11247. DOI: 10.1002/ange.201806823  0.392
2018 Baidilov D, Rycek L, Trant JF, Froese J, Murphy B, Hudlicky T. Innenrücktitelbild: Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin (Angew. Chem. 34/2018) Angewandte Chemie. 130: 11247-11247. DOI: 10.1002/ange.201806823  0.392
2017 Rycek L, Hudlicky T. Applications of the Wittig-Still rearrangement in organic synthesis. Angewandte Chemie (International Ed. in English). PMID 28211171 DOI: 10.1002/Anie.201611329  0.806
2017 Ghavre M, Froese J, Murphy B, Simionescu R, Hudlicky T. A Formal Approach to Xylosmin and Flacourtosides E and F: Chemoenzymatic Total Synthesis of the Hydroxylated Cyclohexenone Carboxylic Acid Moiety of Xylosmin. Organic Letters. PMID 28186763 DOI: 10.1021/Acs.Orglett.7B00194  0.806
2017 Lapinskaite R, Ghavre M, Rintelmann C, Bedard K, Dela Paz H, Hudlicky T. Chemoenzymatic Formal Total Synthesis of Pancratistatin from Narciclasine-Type Compounds via Myers Transposition: Model Study for a Short Conversion of Narciclasine to Pancratistatin Synlett. 28: 2896-2900. DOI: 10.1055/S-0036-1588515  0.821
2017 Lapinskaite R, Ghavre M, Rintelmann C, Bedard K, Dela Paz H, Hudlicky T. Chemoenzymatic Formal Total Synthesis of Pancratistatin from Narciclasine-Type Compounds via Myers Transposition: Model Study for a Short Conversion of Narciclasine to Pancratistatin Synlett. 28: 2896-2900. DOI: 10.1055/s-0036-1588515  0.356
2017 Lapinskaite R, Ghavre M, Rintelmann C, Bedard K, Dela Paz H, Hudlicky T. Chemoenzymatic Formal Total Synthesis of Pancratistatin from Narciclasine-Type Compounds via Myers Transposition: Model Study for a Short Conversion of Narciclasine to Pancratistatin Synlett. 28: 2896-2900. DOI: 10.1055/s-0036-1588515  0.356
2017 Lapinskaite R, Ghavre M, Rintelmann C, Bedard K, Dela Paz H, Hudlicky T. Chemoenzymatic Formal Total Synthesis of Pancratistatin from Narciclasine-Type Compounds via Myers Transposition: Model Study for a Short Conversion of Narciclasine to Pancratistatin Synlett. 28: 2896-2900. DOI: 10.1055/s-0036-1588515  0.356
2017 Lapinskaite R, Ghavre M, Rintelmann C, Bedard K, Dela Paz H, Hudlicky T. Chemoenzymatic Formal Total Synthesis of Pancratistatin from Narciclasine-Type Compounds via Myers Transposition: Model Study for a Short Conversion of Narciclasine to Pancratistatin Synlett. 28: 2896-2900. DOI: 10.1055/s-0036-1588515  0.356
2017 Rycek L, Hudlicky T. Anwendungen der Wittig-Still-Umlagerung in der organischen Synthese Angewandte Chemie. 129: 6118-6162. DOI: 10.1002/Ange.201611329  0.322
2016 Rycek L, Hayward JJ, Latif MA, Tanko J, Simionescu R, Hudlicky T. Chemoenzymatic total synthesis of hydromorphone by an oxidative dearomatization/intramolecular [4+2] cycloaddition sequence: a 2nd generation approach. The Journal of Organic Chemistry. PMID 27690149 DOI: 10.1021/Acs.Joc.6B01990  0.823
2016 Hudlicky T, Endoma-Arias MA. Chemoenzymatic total synthesis of (+)-galanthamine and (+)-narwedine from phenethylacetate. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27505136 DOI: 10.1002/Chem.201603735  0.501
2016 Ghavre M, Froese J, Pour M, Hudlicky T. Synthesis of Amaryllidaceae Constituents and Unnatural Derivatives. Angewandte Chemie (International Ed. in English). PMID 26969844 DOI: 10.1002/Anie.201508227  0.806
2016 Froese J, Overbeeke C, Hudlicky T. Chemoenzymatic synthesis of antiproliferative trihydroxyalkylcyclohexenone isolated from Pleiogynium timorense. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26956129 DOI: 10.1002/Chem.201601061  0.412
2016 Hudlicky T, Ann A. Endoma-Arias M, Machara A, Phillip Cox D. Synthesis of Noroxymorphone by N-Demethylation/ Intramolecular Acylation of Oxymorphone Catalyzed by Iron(II) Chloride Heterocycles. 93: 824. DOI: 10.3987/Com-15-S(T)63  0.717
2016 Šnajdr I, Froese J, Dudding T, Horáková P, Hudlický T. Investigation of a new chiral auxiliary derived chemoenzymatically from toluene: experimental and computational study Canadian Journal of Chemistry. 94: 848-856. DOI: 10.1139/Cjc-2016-0327  0.303
2016 Šnajdr I, Froese J, Dudding T, Horáková P, Hudlický T. Investigation of a new chiral auxiliary derived chemoenzymatically from toluene: experimental and computational study Canadian Journal of Chemistry. 94: 848-856. DOI: 10.1139/Cjc-2016-0327  0.303
2016 Šnajdr I, Froese J, Dudding T, Horáková P, Hudlický T. Investigation of a new chiral auxiliary derived chemoenzymatically from toluene: experimental and computational study Canadian Journal of Chemistry. 94: 848-856. DOI: 10.1139/cjc-2016-0327  0.303
2016 Šnajdr I, Froese J, Dudding T, Horáková P, Hudlický T. Investigation of a new chiral auxiliary derived chemoenzymatically from toluene: experimental and computational study Canadian Journal of Chemistry. 94: 848-856. DOI: 10.1139/cjc-2016-0327  0.303
2016 Šnajdr I, Froese J, Dudding T, Horáková P, Hudlický T. Investigation of a new chiral auxiliary derived chemoenzymatically from toluene: experimental and computational study Canadian Journal of Chemistry. 94: 848-856. DOI: 10.1139/cjc-2016-0327  0.303
2016 Šnajdr I, Froese J, Dudding T, Horáková P, Hudlický T. Investigation of a new chiral auxiliary derived chemoenzymatically from toluene: experimental and computational study Canadian Journal of Chemistry. 94: 848-856. DOI: 10.1139/cjc-2016-0327  0.303
2016 Šnajdr I, Froese J, Dudding T, Horáková P, Hudlický T. Investigation of a new chiral auxiliary derived chemoenzymatically from toluene: experimental and computational study Canadian Journal of Chemistry. 94: 848-856. DOI: 10.1139/cjc-2016-0327  0.303
2016 Šnajdr I, Froese J, Dudding T, Horáková P, Hudlický T. Investigation of a new chiral auxiliary derived chemoenzymatically from toluene: experimental and computational study Canadian Journal of Chemistry. 94: 848-856. DOI: 10.1139/cjc-2016-0327  0.303
2016 Machara A, Hudlický T, Endoma-Arias M, Císařova I, Cox D. Synthesis of Nororipavine and Noroxymorphone via N- and O-Demethylation of Iron Tricarbonyl Complex of Thebaine Synthesis. 48: e1-e1. DOI: 10.1055/S-0035-1562345  0.686
2016 Machara A, Hudlický T, Endoma-Arias M, Císařova I, Cox D. Synthesis of Nororipavine and Noroxymorphone via N- and O-Demethylation of Iron Tricarbonyl Complex of Thebaine Synthesis. 48: e1-e1. DOI: 10.1055/S-0035-1562345  0.686
2016 Albiñana CB, Hayward JJ, Hudlicky T, Machara A. Reinvestigation of acetylation of 3,4-dihydroxybenzaldehyde and reconciliation of previously reported analytical data Tetrahedron Letters. 57: 1019-1021. DOI: 10.1016/J.Tetlet.2016.01.075  0.668
2016 Naoum R, Séguin JP, Trant JF, Frampton MB, Hudlický T, Zelisko PM. A chemoenzymatic route to chiral siloxanes Tetrahedron. 72: 4027-4031. DOI: 10.1016/J.Tet.2016.05.032  0.622
2016 Hudlicky T. Contributions of Ernest Wenkert to the Use of Cyclopropanes in Synthesis – Impact, Reflections, and Recollections Israel Journal of Chemistry. 56: 540-552. DOI: 10.1002/Ijch.201500081  0.352
2016 Machara A, Endoma-Arias MAA, Císařová I, Cox DP, Hudlicky T. Direct Synthesis of Noroxymorphone from Thebaine: Unusual CeIV Oxidation of a Methoxydiene-Iron Complex to an Enone-γ-Nitrate European Journal of Organic Chemistry. 2016: 1500-1503. DOI: 10.1002/Ejoc.201600153  0.716
2016 Machara A, Endoma-Arias MAA, Cisarova I, Cox DP, Hudlicky T. ChemInform Abstract: Direct Synthesis of Noroxymorphone from Thebaine: Unusual CeIVOxidation of a Methoxydiene-Iron Complex to an Enone-γ-nitrate. Cheminform. 47. DOI: 10.1002/chin.201619181  0.686
2016 Ghavre M, Froese J, Pour M, Hudlicky T. Synthese von Inhaltsstoffen der Amaryllisgewächse und nichtnatürlichen Derivaten Angewandte Chemie. 128: 5732-5784. DOI: 10.1002/Ange.201508227  0.782
2015 Qu Y, Easson ML, Froese J, Simionescu R, Hudlicky T, De Luca V. Completion of the seven-step pathway from tabersonine to the anticancer drug precursor vindoline and its assembly in yeast. Proceedings of the National Academy of Sciences of the United States of America. 112: 6224-9. PMID 25918424 DOI: 10.1073/Pnas.1501821112  0.313
2015 Reed JW, Hudlicky T. The quest for a practical synthesis of morphine alkaloids and their derivatives by chemoenzymatic methods. Accounts of Chemical Research. 48: 674-87. PMID 25730681 DOI: 10.1021/Ar500427K  0.608
2015 Hudlicky T. Recent advances in process development for opiate-derived pharmaceutical agents Canadian Journal of Chemistry. 93: 492-501. DOI: 10.1139/Cjc-2014-0552  0.335
2015 Machara A, Werner L, Leisch H, Carroll RJ, Adams DR, Haque DM, Cox DP, Hudlicky T. Synthesis of Naltrexone and (R)-Methylnaltrexone from Oripavine via Direct Oxidation of Its Quaternary Salts Synlett. 26: 2101-2108. DOI: 10.1055/S-0034-1378808  0.765
2014 Froese J, Hudlicky JR, Hudlicky T. Palladium-catalyzed carbonylation of halo arene-cis-dihydrodiols to the corresponding carboxylates. Access to compounds unavailable by toluene dioxygenase-mediated dihydroxylation of the corresponding benzoate esters. Organic & Biomolecular Chemistry. 12: 7810-9. PMID 25158114 DOI: 10.1039/C4Ob01417K  0.405
2014 Vshyvenko S, Reisenauer MR, Rogelj S, Hudlicky T. Synthesis and biological evaluation of unnatural derivatives of narciclasine: 7-aza-nornarciclasine and its N-oxide. Bioorganic & Medicinal Chemistry Letters. 24: 4236-8. PMID 25108300 DOI: 10.1016/J.Bmcl.2014.07.034  0.44
2014 Varghese V, Hudlicky T. Short chemoenzymatic total synthesis of ent-hydromorphone: an oxidative dearomatization/intramolecular [4+2] cycloaddition/amination sequence. Angewandte Chemie (International Ed. in English). 53: 4355-8. PMID 24644041 DOI: 10.1002/Anie.201400286  0.468
2014 Hudlicky T, R. Adams D, van Kempen J, R. Hudlicky J. Chemoenzymatic Approach to Synthesis of Hydroxylated Pyrrolidines from Benzoic Acid Heterocycles. 88: 1255. DOI: 10.3987/Com-13-S(S)89  0.387
2014 Hudlicky T, Trant J, Ho H. The chiro-Inositols and Related Cyclitols as Chiral Monomers for Polymerization: Expansion of a Family of Chiral Polymers Synlett. 25: 2360-2364. DOI: 10.1055/S-0034-1378563  0.609
2014 Froese J, Endoma-Arias MAA, Hudlicky T. Processing of o -halobenzoates by toluene dioxygenase. the role of the alkoxy functionality in the regioselectivity of the enzymatic dihydroxylation reaction Organic Process Research and Development. 18: 801-809. DOI: 10.1021/Op400343C  0.37
2014 Vshyvenko S, Reed JW, Hudlicky T, Piers E. Rearrangements of Vinylcyclopropanes, Divinylcyclopropanes, and Related Systems Comprehensive Organic Synthesis: Second Edition. 5: 999-1076. DOI: 10.1016/B978-0-08-097742-3.00523-1  0.415
2014 Varghese V, Hudlicky T. Cover Picture: Short Chemoenzymatic Total Synthesis ofent-Hydromorphone: An Oxidative Dearomatization/Intramolecular [4+2] Cycloaddition/Amination Sequence (Angew. Chem. Int. Ed. 17/2014) Angewandte Chemie International Edition. 53: 4251-4251. DOI: 10.1002/Anie.201401117  0.389
2014 Varghese V, Hudlicky T. Titelbild: Short Chemoenzymatic Total Synthesis ofent-Hydromorphone: An Oxidative Dearomatization/Intramolecular [4+2] Cycloaddition/Amination Sequence (Angew. Chem. 17/2014) Angewandte Chemie. 126: 4337-4337. DOI: 10.1002/Ange.201401117  0.396
2014 Vshyvenko S, W'Giorgis Z, Weber A, Neverova N, Hedberg B, Hudlicky T. Synthesis and biological activity of 10-aza-narciclasine Advanced Synthesis and Catalysis. 357: 83-87. DOI: 10.1002/Adsc.201400993  0.418
2014 Murphy B, Šnajdr I, Machara A, Endoma-Arias MAA, Stamatatos TC, Cox DP, Hudlický T. Conversion of thebaine to oripavine and other useful intermediates for the semisynthesis of opiate-derived agents: Synthesis of hydromorphone Advanced Synthesis and Catalysis. 356: 2679-2687. DOI: 10.1002/Adsc.201400445  0.734
2014 Endoma-Arias MAA, Hudlicky JR, Simionescu R, Hudlicky T. Chemoenzymatic formal total synthesis of ent-codeine and other morphinans via nitrone cycloadditions and/or radical cyclizations. comparison of strategies for control of C-9/C-14 stereogenic centers Advanced Synthesis and Catalysis. 356: 333-339. DOI: 10.1002/Adsc.201400016  0.412
2013 Winter DK, Endoma-Arias MA, Hudlicky T, Beutler JA, Porco JA. Enantioselective total synthesis and biological evaluation of (+)-kibdelone A and a tetrahydroxanthone analogue. The Journal of Organic Chemistry. 78: 7617-26. PMID 23834060 DOI: 10.1021/Jo401169Z  0.469
2013 Giacometti RD, Duchek J, Werner L, Husni AS, McCurdy CR, Cutler SJ, Cox DP, Hudlicky T. Heteroatom analogues of hydrocodone: synthesis and biological activity. The Journal of Organic Chemistry. 78: 2914-25. PMID 23397939 DOI: 10.1021/Jo3026753  0.613
2013 Trant JF, Hudlicky T. Ring-opening of hindered cyclic epoxides with potassium carboxylates in the presence of conjugate acids Canadian Journal of Chemistry. 91: 1179-1185. DOI: 10.1139/cjc-2013-0386  0.624
2013 Varghese V, Hudlicky T. Total synthesis of dihydrocodeine and hydrocodone via a double claisen rearrangement and C-10/C-11 closure strategy Synlett. 24: 369-374. DOI: 10.1055/S-0032-1318114  0.372
2013 Trant JF, Froese J, Hudlicky T. Enzymatic oxidation of para-substituted arenes: Access to new non-racemic chiral metabolites for synthesis Tetrahedron Asymmetry. 24: 184-190. DOI: 10.1016/J.Tetasy.2013.01.002  0.709
2013 Endoma-Arias MAA, Cox DP, Hudlicky T. General method of synthesis for naloxone, naltrexone, nalbuphone, and nalbuphine by the reaction of grignard reagents with an oxazolidine derived from oxymorphone Advanced Synthesis and Catalysis. 355: 1869-1873. DOI: 10.1002/Adsc.201300284  0.413
2012 Vshyvenko S, Scattolon J, Hudlicky T, Romero AE, Kornienko A, Ma D, Tuffley I, Pandey S. Unnatural C-1 homologues of pancratistatin - Synthesis and promising biological activities. Canadian Journal of Chemistry. 90: 932-943. PMID 28017970 DOI: 10.1139/V2012-073  0.387
2012 Semak V, Metcalf TA, Endoma-Arias MA, Mach P, Hudlicky T. Toluene dioxygenase mediated oxidation of halogen-substituted benzoate esters. Organic & Biomolecular Chemistry. 10: 4407-16. PMID 22562668 DOI: 10.1039/C2Ob25202C  0.361
2012 Rinner U, Hudlicky T. Synthesis of morphine alkaloids and derivatives. Topics in Current Chemistry. 309: 33-66. PMID 21547687 DOI: 10.1007/128_2011_133  0.741
2012 Trant JF, Belding L, Dudding T, Hudlicky T. Application of D-chiro-inositol as a chiral template for the diels-alder reaction Helvetica Chimica Acta. 95: 2026-2035. DOI: 10.1002/Hlca.201200432  0.665
2012 Carlson R, Hudlicky T. On hype, malpractice, and scientific misconduct in organic synthesis Helvetica Chimica Acta. 95: 2052-2062. DOI: 10.1002/Hlca.201200431  0.348
2012 MacHara A, Cox DP, Hudlicky T. Direct synthesis of naltrexone by palladium-catalyzed N-demethylation/ acylation of oxymorphone: The benefit of C-H activation and the intramolecular acyl transfer from C-14 hydroxy Advanced Synthesis and Catalysis. 354: 2713-2718. DOI: 10.1002/Adsc.201200677  0.712
2012 Werner L, Wernerova M, MacHara A, Endoma-Arias MA, Duchek J, Adams DR, Cox DP, Hudlicky T. Unexpected N-demethylation of oxymorphone and oxycodone N-oxides mediated by the burgess reagent: Direct synthesis of naltrexone, naloxone, and other antagonists from oxymorphone Advanced Synthesis and Catalysis. 354: 2706-2712. DOI: 10.1002/Adsc.201200676  0.794
2012 MacHara A, Werner L, Endoma-Arias MA, Cox DP, Hudlicky T. Improved synthesis of buprenorphine from thebaine and/or oripavine via palladium-catalyzed N-demethylation/acylation and/or concomitant O-demethylation Advanced Synthesis and Catalysis. 354: 613-626. DOI: 10.1002/Adsc.201100807  0.783
2011 Werner L, Machara A, Sullivan B, Carrera I, Moser M, Adams DR, Hudlicky T, Andraos J. Several generations of chemoenzymatic synthesis of oseltamivir (Tamiflu): evolution of strategy, quest for a process-quality synthesis, and evaluation of efficiency metrics. The Journal of Organic Chemistry. 76: 10050-67. PMID 22007598 DOI: 10.1021/Jo2018872  0.814
2011 Vshyvenko S, Scattolon J, Hudlicky T, Romero AE, Kornienko A. Synthesis of C-1 homologues of pancratistatin and their preliminary biological evaluation. Bioorganic & Medicinal Chemistry Letters. 21: 4750-2. PMID 21757350 DOI: 10.1016/J.Bmcl.2011.06.068  0.451
2011 Hudlicky T. Introduction to enzymes in synthesis. Chemical Reviews. 111: 3995-7. PMID 21671674 DOI: 10.1021/Cr200185S  0.345
2011 Duchek J, Adams DR, Hudlicky T. Chemoenzymatic synthesis of inositols, conduritols, and cyclitol analogues. Chemical Reviews. 111: 4223-58. PMID 21630704 DOI: 10.1021/Cr1004138  0.487
2011 Werner L, Machara A, Adams DR, Cox DP, Hudlicky T. Synthesis of buprenorphine from oripavine via N-demethylation of oripavine quaternary salts. The Journal of Organic Chemistry. 76: 4628-34. PMID 21495679 DOI: 10.1021/Jo200567N  0.797
2011 Machara A, Cox DP, Hudlicky T. Synthesis of nalbuphine from oripavine via N-demethylation of N-cyclobutylmethyl oripavine Heterocycles. 84: 615-623. DOI: 10.3987/Com-11-S(P)32  0.697
2011 Hudlicky JR, Werner L, Semak V, Simionescu R, Hudlicky T. Dauben-Michno oxidative transposition of allylic cyanohydrins - Enantiomeric switch of (-)-carvone to (+)-carvone Canadian Journal of Chemistry. 89: 535-543. DOI: 10.1139/v11-026  0.507
2011 Hudlicky JR, Hopkins-Hill J, Hudlicky T. Explorations of [4+2] and [5+2] cycloadditions of dienylcyclopropane derived enzymatically from cyclopropylbenzene Synlett. 2891-2895. DOI: 10.1055/S-0031-1289553  0.357
2011 Werner L, Machara A, Adams DR, Cox DP, Hudlicky T. Synthesis of Buprenorphine Synfacts. 2011: 817-817. DOI: 10.1055/S-0030-1260675  0.813
2011 Adams DR, Aichinger C, Rinner U, Hudlicky T. Chemoenzymatic synthesis of idesolide from benzoic acid Synlett. 725-729. DOI: 10.1055/S-0030-1259694  0.712
2011 Adams DR, Aichinger C, Collins J, Rinner U, Hudlicky T. Addendum Synlett. 1188. DOI: 10.1055/s-0029-1260550  0.587
2011 Endoma-Arias MAA, Hudlicky T. A short synthesis of nonracemic iodocyclohexene carboxylate fragment for kibdelone and congeners Tetrahedron Letters. 52: 6632-6634. DOI: 10.1016/J.Tetlet.2011.10.005  0.453
2010 Hudlicky T, Reed JW. From discovery to application: 50 years of the vinylcyclopropane-cyclopentene rearrangement and its impact on the synthesis of natural products. Angewandte Chemie (International Ed. in English). 49: 4864-76. PMID 20586104 DOI: 10.1002/Anie.200906001  0.586
2010 Collins J, Rinner U, Moser M, Hudlicky T, Ghiviriga I, Romero AE, Kornienko A, Ma D, Griffin C, Pandey S. Chemoenzymatic synthesis of Amaryllidaceae constituents and biological evaluation of their C-1 analogues. The next generation synthesis of 7-deoxypancratistatin and trans-dihydrolycoricidine. The Journal of Organic Chemistry. 75: 3069-84. PMID 20373760 DOI: 10.1021/Jo1003136  0.751
2010 Werner L, Hudlicky JR, Wernerova M, Hudlicky T. Synthesis of 1,2- and 1,4-amino alcohols from 1,3-dienes via oxazines. Rearrangements of 1,4-amino alcohol derivatives to oxazolines Tetrahedron. 66: 3761-3769. DOI: 10.1016/J.Tet.2010.03.059  0.569
2010 Zezula J, Hudlicky T, Ghiviriga I. ChemInform Abstract: Intramolecular Diels-Alder Cycloadditions of cis-Cyclohexadienediols Derived Enzymatically from (2-Azidoethyl)benzene. Construction of Highly Functionalized Bridged Isoquinoline Synthons. Cheminform. 33: no-no. DOI: 10.1002/chin.200207139  0.692
2010 Paul BJ, Hobbs E, Buccino P, Hudlicky T. ChemInform Abstract: Opening of a Vinyl Aziridine with p-Toluenesulfonamide under TBAF Catalysis: Synthesis of 3,4-Diamino-3,4-dideoxy-L-chiro-inositol. Cheminform. 33: no-no. DOI: 10.1002/chin.200202216  0.534
2010 Bottari P, Endoma MAA, Hudlicky T, Ghiviriga I, Abboud KA. ChemInform Abstract: Intramolecular N-Acyliminium Ion-Olefin Cyclization in the Synthesis of Optically Pure Isoquinoline Derivatives: Control of Stereochemistry and Application to Synthesis of Morphine Alkaloids. Cheminform. 30: no-no. DOI: 10.1002/chin.199931254  0.314
2010 Bottari P, Endoma MAA, Hudlicky T, Ghiviriga I, Abboud KA. ChemInform Abstract: Intramolecular N-Acyliminium Ion-Olefin Cyclization in the Synthesis of Optically Pure Isoquinoline Derivatives: Control of Stereochemistry and Application to Synthesis of Morphine Alkaloids. Cheminform. 30: no-no. DOI: 10.1002/chin.199931254  0.314
2010 Bottari P, Endoma MAA, Hudlicky T, Ghiviriga I, Abboud KA. ChemInform Abstract: Intramolecular N-Acyliminium Ion-Olefin Cyclization in the Synthesis of Optically Pure Isoquinoline Derivatives: Control of Stereochemistry and Application to Synthesis of Morphine Alkaloids. Cheminform. 30: no-no. DOI: 10.1002/chin.199931254  0.314
2010 Bottari P, Endoma MAA, Hudlicky T, Ghiviriga I, Abboud KA. ChemInform Abstract: Intramolecular N-Acyliminium Ion-Olefin Cyclization in the Synthesis of Optically Pure Isoquinoline Derivatives: Control of Stereochemistry and Application to Synthesis of Morphine Alkaloids. Cheminform. 30: no-no. DOI: 10.1002/chin.199931254  0.314
2010 Bottari P, Endoma MAA, Hudlicky T, Ghiviriga I, Abboud KA. ChemInform Abstract: Intramolecular N-Acyliminium Ion-Olefin Cyclization in the Synthesis of Optically Pure Isoquinoline Derivatives: Control of Stereochemistry and Application to Synthesis of Morphine Alkaloids. Cheminform. 30: no-no. DOI: 10.1002/chin.199931254  0.314
2010 Bottari P, Endoma MAA, Hudlicky T, Ghiviriga I, Abboud KA. ChemInform Abstract: Intramolecular N-Acyliminium Ion-Olefin Cyclization in the Synthesis of Optically Pure Isoquinoline Derivatives: Control of Stereochemistry and Application to Synthesis of Morphine Alkaloids. Cheminform. 30: no-no. DOI: 10.1002/chin.199931254  0.314
2010 Bottari P, Endoma MAA, Hudlicky T, Ghiviriga I, Abboud KA. ChemInform Abstract: Intramolecular N-Acyliminium Ion-Olefin Cyclization in the Synthesis of Optically Pure Isoquinoline Derivatives: Control of Stereochemistry and Application to Synthesis of Morphine Alkaloids. Cheminform. 30: no-no. DOI: 10.1002/chin.199931254  0.314
2010 Bottari P, Endoma MAA, Hudlicky T, Ghiviriga I, Abboud KA. ChemInform Abstract: Intramolecular N-Acyliminium Ion-Olefin Cyclization in the Synthesis of Optically Pure Isoquinoline Derivatives: Control of Stereochemistry and Application to Synthesis of Morphine Alkaloids. Cheminform. 30: no-no. DOI: 10.1002/chin.199931254  0.314
2010 HUDLICKY T, REED JW. ChemInform Abstract: An Evolutionary Perspective of Microbial Oxidations of Aromatic Compounds in Enantioselective Synthesis: History, Current Status, and Perspectives Cheminform. 28: no-no. DOI: 10.1002/chin.199709228  0.57
2010 TIAN X, MAURYA R, KOENIGSBERGER K, HUDLICKY T. ChemInform Abstract: Asymmetric Total Synthesis of (+)-7-Deoxypancratistatin. Cheminform. 27: no-no. DOI: 10.1002/chin.199616252  0.373
2010 TIAN X, MAURYA R, KOENIGSBERGER K, HUDLICKY T. ChemInform Abstract: Asymmetric Total Synthesis of (+)-7-Deoxypancratistatin. Cheminform. 27: no-no. DOI: 10.1002/chin.199616252  0.373
2010 TIAN X, MAURYA R, KOENIGSBERGER K, HUDLICKY T. ChemInform Abstract: Asymmetric Total Synthesis of (+)-7-Deoxypancratistatin. Cheminform. 27: no-no. DOI: 10.1002/chin.199616252  0.373
2010 TIAN X, MAURYA R, KOENIGSBERGER K, HUDLICKY T. ChemInform Abstract: Asymmetric Total Synthesis of (+)-7-Deoxypancratistatin. Cheminform. 27: no-no. DOI: 10.1002/chin.199616252  0.373
2010 TIAN X, MAURYA R, KOENIGSBERGER K, HUDLICKY T. ChemInform Abstract: Asymmetric Total Synthesis of (+)-7-Deoxypancratistatin. Cheminform. 27: no-no. DOI: 10.1002/chin.199616252  0.373
2010 TIAN X, MAURYA R, KOENIGSBERGER K, HUDLICKY T. ChemInform Abstract: Asymmetric Total Synthesis of (+)-7-Deoxypancratistatin. Cheminform. 27: no-no. DOI: 10.1002/chin.199616252  0.373
2010 TIAN X, MAURYA R, KOENIGSBERGER K, HUDLICKY T. ChemInform Abstract: Asymmetric Total Synthesis of (+)-7-Deoxypancratistatin. Cheminform. 27: no-no. DOI: 10.1002/chin.199616252  0.373
2010 TIAN X, MAURYA R, KOENIGSBERGER K, HUDLICKY T. ChemInform Abstract: Asymmetric Total Synthesis of (+)-7-Deoxypancratistatin. Cheminform. 27: no-no. DOI: 10.1002/chin.199616252  0.373
2010 MANDEL M, HUDLICKY T. ChemInform Abstract: Conduritolhalo Epoxides: Versatile Synthons for Cyclitol Synthesis. Cheminform. 25: no-no. DOI: 10.1002/chin.199405262  0.396
2010 MANDEL M, HUDLICKY T. ChemInform Abstract: Conduritolhalo Epoxides: Versatile Synthons for Cyclitol Synthesis. Cheminform. 25: no-no. DOI: 10.1002/chin.199405262  0.396
2010 MANDEL M, HUDLICKY T. ChemInform Abstract: Conduritolhalo Epoxides: Versatile Synthons for Cyclitol Synthesis. Cheminform. 25: no-no. DOI: 10.1002/chin.199405262  0.396
2010 MANDEL M, HUDLICKY T. ChemInform Abstract: Conduritolhalo Epoxides: Versatile Synthons for Cyclitol Synthesis. Cheminform. 25: no-no. DOI: 10.1002/chin.199405262  0.396
2010 MANDEL M, HUDLICKY T. ChemInform Abstract: Conduritolhalo Epoxides: Versatile Synthons for Cyclitol Synthesis. Cheminform. 25: no-no. DOI: 10.1002/chin.199405262  0.396
2010 MANDEL M, HUDLICKY T. ChemInform Abstract: Conduritolhalo Epoxides: Versatile Synthons for Cyclitol Synthesis. Cheminform. 25: no-no. DOI: 10.1002/chin.199405262  0.396
2010 MANDEL M, HUDLICKY T. ChemInform Abstract: Conduritolhalo Epoxides: Versatile Synthons for Cyclitol Synthesis. Cheminform. 25: no-no. DOI: 10.1002/chin.199405262  0.396
2010 MANDEL M, HUDLICKY T. ChemInform Abstract: Conduritolhalo Epoxides: Versatile Synthons for Cyclitol Synthesis. Cheminform. 25: no-no. DOI: 10.1002/chin.199405262  0.396
2010 HUDLICKY T, FAN R, LUNA H, OLIVO H, PRICE J. ChemInform Abstract: Enzymatic Hydroxylation of Arene and Symmetry Considerations in Efficient Synthetic Design of Oxygenated Natural Products Cheminform. 24: no-no. DOI: 10.1002/chin.199318323  0.587
2010 HUDLICKY T, OLIVO HF. ChemInform Abstract: A Short Synthesis of (+)-Lycoricidine. Cheminform. 24: no-no. DOI: 10.1002/chin.199314277  0.353
2010 HUDLICKY T, OLIVO HF. ChemInform Abstract: A Short Synthesis of (+)-Lycoricidine. Cheminform. 24: no-no. DOI: 10.1002/chin.199314277  0.353
2010 HUDLICKY T, OLIVO HF. ChemInform Abstract: A Short Synthesis of (+)-Lycoricidine. Cheminform. 24: no-no. DOI: 10.1002/chin.199314277  0.68
2010 HUDLICKY T, OLIVO HF. ChemInform Abstract: Stereospecific Synthesis of Aminocyclitols via Cycloadditions of Unsymmetrical, Optically Pure Dienes: Conduramine A-1 and Dihydroconduramine A-1. Cheminform. 23: no-no. DOI: 10.1002/chin.199227079  0.633
2010 HUDLICKY T, LUNA H, OLIVO HF, ANDERSEN C, NUGENT T, PRICE JD. ChemInform Abstract: Biocatalysis as the Strategy of Choice in the Exhaustive Enantiomerically Controlled Synthesis of Conduritols. Cheminform. 23: no-no. DOI: 10.1002/chin.199213297  0.639
2010 HUDLICKY T, PRICE JD, OLIVO HF. ChemInform Abstract: Enantiocontrolled Total Synthesis of Conduritols: (+)-Conduritol E (I) and (-)-Conduritol F (II). Cheminform. 23: no-no. DOI: 10.1002/chin.199204054  0.597
2010 HUDLICKY T, PRICE JD, RULIN F, TSUNODA T. ChemInform Abstract: Efficient and Enantiodivergent Synthesis of (+)- and (-)-Pinitol. Cheminform. 22: no-no. DOI: 10.1002/chin.199112319  0.336
2010 HUDLICKY T, PRICE JD, RULIN F, TSUNODA T. ChemInform Abstract: Efficient and Enantiodivergent Synthesis of (+)- and (-)-Pinitol. Cheminform. 22: no-no. DOI: 10.1002/chin.199112319  0.336
2010 HUDLICKY T, PRICE JD, RULIN F, TSUNODA T. ChemInform Abstract: Efficient and Enantiodivergent Synthesis of (+)- and (-)-Pinitol. Cheminform. 22: no-no. DOI: 10.1002/chin.199112319  0.336
2010 HUDLICKY T, PRICE JD, RULIN F, TSUNODA T. ChemInform Abstract: Efficient and Enantiodivergent Synthesis of (+)- and (-)-Pinitol. Cheminform. 22: no-no. DOI: 10.1002/chin.199112319  0.336
2010 HUDLICKY T, PRICE JD, RULIN F, TSUNODA T. ChemInform Abstract: Efficient and Enantiodivergent Synthesis of (+)- and (-)-Pinitol. Cheminform. 22: no-no. DOI: 10.1002/chin.199112319  0.336
2010 HUDLICKY T, SEOANE G, PRICE JD, GADAMASETTI KG. ChemInform Abstract: An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via (4 + 1)Azide-Diene Annulation Methodology Cheminform. 22: no-no. DOI: 10.1002/chin.199102382  0.683
2010 HUDLICKY T, SEOANE G, PRICE JD, GADAMASETTI KG. ChemInform Abstract: An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via (4 + 1)Azide-Diene Annulation Methodology Cheminform. 22: no-no. DOI: 10.1002/chin.199102382  0.397
2010 HUDLICKY T, SEOANE G, PRICE JD, GADAMASETTI KG. ChemInform Abstract: An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via (4 + 1)Azide-Diene Annulation Methodology Cheminform. 22: no-no. DOI: 10.1002/chin.199102382  0.397
2010 HUDLICKY T, SEOANE G, PRICE JD, GADAMASETTI KG. ChemInform Abstract: An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via (4 + 1)Azide-Diene Annulation Methodology Cheminform. 22: no-no. DOI: 10.1002/chin.199102382  0.397
2010 HUDLICKY T, SEOANE G, PRICE JD, GADAMASETTI KG. ChemInform Abstract: An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via (4 + 1)Azide-Diene Annulation Methodology Cheminform. 22: no-no. DOI: 10.1002/chin.199102382  0.397
2010 HUDLICKY T, SEOANE G, PRICE JD, GADAMASETTI KG. ChemInform Abstract: An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via (4 + 1)Azide-Diene Annulation Methodology Cheminform. 22: no-no. DOI: 10.1002/chin.199102382  0.397
2010 HUDLICKY T, SEOANE G, PRICE JD, GADAMASETTI KG. ChemInform Abstract: An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via (4 + 1)Azide-Diene Annulation Methodology Cheminform. 22: no-no. DOI: 10.1002/chin.199102382  0.397
2010 HUDLICKY T, OLIVO HF, NATCHUS MG, UMPIERREZ EF, PANDOLFI E, VOLONTERIO C. ChemInform Abstract: Synthesis of β-Methoxy Enones via a New Two-Carbon Extension of Carboxylic Acids. Cheminform. 22: no-no. DOI: 10.1002/chin.199102165  0.621
2010 Hudlicky T, Reed J. Von der Entdeckung bis zur Anwendung: 50 Jahre Vinylcyclopropan-Cyclopenten-Umlagerung und ihre Bedeutung in der Naturstoffsynthese Angewandte Chemie. 122: 4982-4994. DOI: 10.1002/Ange.200906001  0.512
2010 Werner L, Machara A, Hudlicky T. Short chemoenzymatic azide-free synthesis of oseltamivir (tamiflu): Approaching the potential for process efficiency Advanced Synthesis and Catalysis. 352: 195-200. DOI: 10.1002/Adsc.200900844  0.799
2009 Hudlicky T, Reed JW. Applications of biotransformations and biocatalysis to complexity generation in organic synthesis. Chemical Society Reviews. 38: 3117-32. PMID 19847346 DOI: 10.1039/B901172M  0.582
2009 Fabris F, Collins J, Sullivan B, Leisch H, Hudlicky T. Investigation of steric and functionality limits in the enzymatic dihydroxylation of benzoate esters. Versatile intermediates for the synthesis of pseudo-sugars, amino cyclitols, and bicyclic ring systems. Organic & Biomolecular Chemistry. 7: 2619-27. PMID 19503938 DOI: 10.1039/B902577B  0.451
2009 Sullivan B, Carrera I, Drouin M, Hudlicky T. Symmetry-based design for the chemoenzymatic synthesis of oseltamivir (Tamiflu) from ethyl benzoate. Angewandte Chemie (International Ed. in English). 48: 4229-31. PMID 19425033 DOI: 10.1002/Anie.200901345  0.758
2009 Carroll RJ, Leisch H, Rochon L, Hudlicky T, Cox DP. One-pot conversion of thebaine to hydrocodone and synthesis of neopinone ketal. The Journal of Organic Chemistry. 74: 747-52. PMID 19072148 DOI: 10.1021/Jo802454V  0.397
2009 Hudlicky T, Reed JW. Celebrating 20 years of Synlett - Special account on the merits of biocatalysis and the impact of arene cis-dihydrodiols on enantioselective synthesis Synlett. 0685-0703. DOI: 10.1055/S-0028-1087946  0.617
2009 Leisch H, Omori AT, Finn KJ, Gilmet J, Bissett T, Ilceski D, Hudlický T. Chemoenzymatic enantiodivergent total syntheses of (+)- and (-)-codeine Tetrahedron. 65: 9862-9875. DOI: 10.1016/J.Tet.2009.09.052  0.818
2009 Leisch H, Omori AT, Finn KJ, Gilmet J, Bissett T, Ilceski D, Hudlický T. Chemoenzymatic enantiodivergent total syntheses of (+)- and (-)-codeine Tetrahedron. 65: 9862-9875. DOI: 10.1016/J.Tet.2009.09.052  0.818
2009 Gilmet J, Sullivan B, Hudlicky T. Formal total synthesis of (-)- and (+)-balanol: two complementary enantiodivergent routes from vinyloxiranes and vinylaziridines Tetrahedron. 65: 212-220. DOI: 10.1016/J.Tet.2008.10.070  0.487
2009 Leisch H, Sullivan B, Fonovic B, Dudding T, Hudlicky T. New options for the reactivity of the burgess reagent with epoxides in both racemic and chiral auxiliary modes - Structural and mechanistic revisions, computational studies, and application to synthesis European Journal of Organic Chemistry. 2806-2819. DOI: 10.1002/Ejoc.200900159  0.418
2008 Sullivan B, Gilmet J, Leisch H, Hudlicky T. Chiral version of the Burgess reagent and its reactions with oxiranes: application to the formal enantiodivergent synthesis of balanol. Journal of Natural Products. 71: 346-50. PMID 18205317 DOI: 10.1021/Np0705357  0.461
2008 Collins J, Drouin M, Sun X, Rinner U, Hudlicky T. Total synthesis of 7-deoxypancratistatin-1-carboxaldehyde and carboxylic acid via solvent-free intramolecular aziridine opening: phenanthrene to phenanthridone cyclization strategy. Organic Letters. 10: 361-4. PMID 18163635 DOI: 10.1021/Ol702440F  0.75
2008 Sullivan B, Hudlicky T. Chemoenzymatic formal synthesis of (-)-balanol. Provision of optical data for an often-reported intermediate Tetrahedron Letters. 49: 5211-5213. DOI: 10.1016/J.Tetlet.2008.06.026  0.381
2008 Saxon RE, Leisch H, Hudlicky T. Preliminary investigation of the yeast-mediated reduction of β-keto amides derived from cyclic amines as potential resolution methodology Tetrahedron Asymmetry. 19: 672-681. DOI: 10.1016/J.Tetasy.2008.02.021  0.313
2007 Banfield SC, Omori AT, Leisch H, Hudlicky T. Unexpected reactivity of the burgess reagent with thiols: synthesis of symmetrical disulfides. The Journal of Organic Chemistry. 72: 4989-92. PMID 17539682 DOI: 10.1021/Jo070099T  0.752
2007 Omori AT, Finn KJ, Leisch H, Carroll RJ, Hudlicky T. Chemoenzymatic total synthesis of (+)-codeine by sequential intramolecular Heck cyclizations via C-B-D ring construction Synlett. 2859-2862. DOI: 10.1055/S-2007-990833  0.823
2007 Zezula J, Rice KC, Hudlicky T. Design for morphine alkaloids by intramolecular Heck strategy: Chemoenzymatic synthesis of 10-hydroxy-14-epi-dihydrocodeinone via C-D-B ring construction Synlett. 2863-2867. DOI: 10.1055/S-2007-990832  0.743
2007 Moser M, Hudlicky T, Sadeghi S, Sternin E. Synthesis of deuterium-labelled chlorhexidine Journal of Labelled Compounds and Radiopharmaceuticals. 50: 671-674. DOI: 10.1002/Jlcr.1383  0.479
2006 Hudlicky T. Chemoenzymatic synthesis of complex natural and unnatural products: Morphine, pancratistatin, and their analogs Arkivoc. 2006: 276-291. DOI: 10.3998/Ark.5550190.0007.720  0.346
2006 Hudlicky T, Moser M, Banfield SC, Rinner U, Chapuis JC, Pettit GR. Cyclotrimerization approach to unnatural structural modifications of pancratistatin and other amaryllidaceae constituents - Synthesis and biological evaluation Canadian Journal of Chemistry. 84: 1313-1337. DOI: 10.1139/V06-078  0.748
2006 Ghosh S, Kinney WA, Gauthier DA, Lawson EC, Hudlicky T, Maryanoff BE. Convenient preparation of aryl-substituted nortropanes by Suzuki-Miyaura methodology Canadian Journal of Chemistry. 84: 555-560. DOI: 10.1139/V06-045  0.436
2006 Leisch H, Saxon R, Sullivan B, Hudlicky T. Chiral version of the Burgess reagent and its reactions with epoxides Synlett. 445-449. DOI: 10.1055/S-2006-932450  0.37
2006 Brugel TA, Hudlicky T, Clark MP, Golebiowski A, Sabat M, Endoma MAA, Bui V, Adams D, Laufersweiler MJ, Maier JA, Bookland RG, De B. Convergent synthesis of 2,3-bisarylpyrazolones through cyclization of bisacylated pyrazolidines and hydrazines Tetrahedron Letters. 47: 3195-3198. DOI: 10.1016/J.Tetlet.2006.03.063  0.753
2006 Finn KJ, Collins J, Hudlicky T. Toluene dioxygenase-mediated oxidation of dibromobenzenes. Absolute stereochemistry of new metabolites and synthesis of (-)-conduritol E Tetrahedron. 62: 7471-7476. DOI: 10.1016/J.Tet.2006.05.012  0.708
2005 Moser M, Sun X, Hudlicky T. Cyclotrimerization strategy toward analogues of amaryllidaceae constituents. synthesis of deoxygenated pancratistatin core. Organic Letters. 7: 5669-72. PMID 16321018 DOI: 10.1021/Ol052372O  0.477
2005 Hudlicky T, Rinner U, Finn KJ, Ghiviriga I. Reactions of indole derivatives with oxiranes and aziridines on silica. Synthesis of beta-carbolin-1-one mimic of pancratistatin. The Journal of Organic Chemistry. 70: 3490-9. PMID 15844982 DOI: 10.1021/Jo040292C  0.824
2005 Finn KJ, Pavlyuk O, Hudlický T. Toluene dioxygenase-mediated oxidation of bromo(methylsulfanyl)benzenes. Absolute configuration of metabolites and evaluation of chemo- and regioselectivity trends Collection of Czechoslovak Chemical Communications. 70: 1709-1726. DOI: 10.1135/Cccc20051709  0.694
2005 Gordon HL, Freeman S, Hudlicky T. Stability relationships in bicyclic ketones Synlett. 2911-2914. DOI: 10.1055/S-2005-918959  0.625
2005 Zezula J, Hudlicky T. Recent progress in the synthesis of morphine alkaloids Synlett. 388-405. DOI: 10.1055/S-2005-862383  0.702
2005 Rinner U, Hudlicky T. Synthesis of amaryllidaceae constituents - An update Synlett. 365-387. DOI: 10.1055/S-2005-862382  0.73
2005 Finn KJ, Rochon L, Hudlicky T. Processing of cyclopropylarenes by toluene dioxygenase: Isolation and absolute configuration of metabolites Tetrahedron Asymmetry. 16: 3606-3613. DOI: 10.1016/J.Tetasy.2005.09.020  0.674
2005 Hudlicky T, Rinner U, Finn KJ, Ghiviriga I. Reactions of Indole Derivatives with Oxiranes and Aziridines on Silica. Synthesis of a β-Carbolin-1-one Mimic (XIII) of Pancratistatin. Cheminform. 36. DOI: 10.1002/chin.200538124  0.693
2004 Rinner U, Hudlicky T, Gordon H, Pettit GR. A beta-carboline-1-one mimic of the anticancer Amaryllidaceae constituent pancratistatin: synthesis and biological evaluation. Angewandte Chemie (International Ed. in English). 43: 5342-6. PMID 15468184 DOI: 10.1002/Anie.200460218  0.684
2004 Rinner U, Hillebrenner HL, Adams DR, Hudlicky T, Pettit GR. Synthesis and biological activity of some structural modifications of pancratistatin. Bioorganic & Medicinal Chemistry Letters. 14: 2911-5. PMID 15125958 DOI: 10.1016/J.Bmcl.2004.03.032  0.692
2004 Freeman S, Hudlicky T. New oligomers of conduritol-F and muco-inositol. Synthesis and biological evaluation as glycosidase inhibitors. Bioorganic & Medicinal Chemistry Letters. 14: 1209-12. PMID 14980667 DOI: 10.1016/J.Bmcl.2003.12.050  0.63
2004 Finn KJ, Canka? P, Jones TRB, Hudlicky T. Enzymatic oxidation of thioanisoles: Isolation and absolute configuration of metabolites Tetrahedron Asymmetry. 15: 2833-2836. DOI: 10.1016/J.Tetasy.2004.06.050  0.689
2004 Newman LM, Garcia H, Hudlicky T, Selifonov SA. Directed evolution of the dioxygenase complex for the synthesis of furanone flavor compounds Tetrahedron. 60: 729-734. DOI: 10.1016/J.Tet.2003.10.105  0.427
2004 Bui VP, Hudlicky T. Synthesis of chiral ADMET polymers containing repeating D-chiro-inositol units derived from a biocatalytically prepared diene diol Tetrahedron. 60: 641-646. DOI: 10.1016/J.Tet.2003.10.097  0.713
2004 Yildirim S, Zezula J, Hudlicky T, Witholt B, Schmid A. Asymmetric dihydroxylation of cinnamonitrile to trans-3-[(5S,6R)-5,6- dihydroxycyclohexa-1,3-dienyl]-acrylonitrile using chlorobenzene dioxygenase in Escherichia coli (pTEZ30) Advanced Synthesis and Catalysis. 346: 933-942. DOI: 10.1002/Adsc.200404032  0.684
2004 Hudlicky T, Fan R, Reed JW, Gadamasetti KG. Divinylcyclopropane‐Cycloheptadiene Rearrangement Organic Reactions. 1-133. DOI: 10.1002/0471264180.Or041.01  0.402
2003 Hudlicky T. PREFACE [Hot topic: Asymmetric Synthesis (Guest Editor: Tomas Hudlicky)] Current Organic Chemistry. 7: i-i. DOI: 10.2174/1385272033486206  0.461
2003 Hudlicky T. PREFACE [Hot topic: Asymmetric Synthesis (Guest Editor: Tomas Hudlicky)] Current Organic Chemistry. 7: i-i. DOI: 10.2174/1385272033486206  0.354
2003 Hudlicky T. PREFACE [Hot topic: Asymmetric Synthesis (Guest Editor: Tomas Hudlicky)] Current Organic Chemistry. 7: i-i. DOI: 10.2174/1385272033486206  0.354
2003 Hudlicky T. PREFACE [Hot topic: Asymmetric Synthesis (Guest Editor: Tomas Hudlicky)] Current Organic Chemistry. 7: i-i. DOI: 10.2174/1385272033486206  0.354
2003 Hudlicky T. PREFACE [Hot topic: Asymmetric Synthesis (Guest Editor: Tomas Hudlicky)] Current Organic Chemistry. 7: i-i. DOI: 10.2174/1385272033486206  0.354
2003 Rinner U, Adams DR, Dos Santos ML, Abboud KA, Hudlicky T. New application of Burgess reagent in its reaction with epoxides Synlett. 1247-1252. DOI: 10.1055/S-2003-40356  0.719
2003 Hansen J, Freeman S, Hudlicky T. Selective electrochemical deprotection of cinnamyl ethers, esters, and carbamates Tetrahedron Letters. 44: 1575-1578. DOI: 10.1016/S0040-4039(03)00009-1  0.596
2003 Rigby HL, Neveu M, Pauley D, Ranu BC, Hudlicky T. 3‐Hydroxy‐1‐cyclohexene‐1‐carboxaldehyde Organic Syntheses. 205-205. DOI: 10.1002/0471264180.Os067.28  0.669
2003 Pauley D, Anderson F, Hudlicky T. 4,4‐Dimethyl‐2‐Cyclopenten‐1‐one Organic Syntheses. 121-121. DOI: 10.1002/0471264180.Os067.15  0.337
2002 Hudlicky T, Rinner U, Gonzalez D, Akgun H, Schilling S, Siengalewicz P, Martinot TA, Pettit GR. Total synthesis and biological evaluation of Amaryllidaceae alkaloids: narciclasine, ent-7-deoxypancratistatin, regioisomer of 7-deoxypancratistatin, 10b-epi-deoxypancratistatin, and truncated derivatives. The Journal of Organic Chemistry. 67: 8726-43. PMID 12467383 DOI: 10.1021/Jo020129M  0.815
2002 Paul BJ, Willis J, Martinot TA, Ghiviriga I, Abboud KA, Hudlicky T. Synthesis, structure, and biological evaluation of novel N- and O-linked diinositols. Journal of the American Chemical Society. 124: 10416-26. PMID 12197743 DOI: 10.1021/Ja0205378  0.789
2002 Rinner U, Siengalewicz P, Hudlicky T. Total synthesis of epi-7-deoxypancratistatin via aza-Payne rearrangement and intramolecular cyclization. Organic Letters. 4: 115-7. PMID 11772104 DOI: 10.1021/Ol0169877  0.764
2002 Bui VP, Nguyen M, Hansen J, Baker J, Hudlicky T. Enzymatic oxidation of cyclopropylbenzene: Structures of new metabolites and possible mechanistic implications Canadian Journal of Chemistry. 80: 708-713. DOI: 10.1139/V02-098  0.732
2002 Endoma MA, Bui VP, Hansen J, Hudlicky T. Medium-scale preparation of useful metabolites of aromatic compounds via whole-cell fermentation with recombinant organisms Organic Process Research and Development. 6: 525-532. DOI: 10.1021/Op020013S  0.689
2002 Rinner U, Siengalewicz P, Hudlicky T. Total synthesis of epi-7-deoxypancratistatin via aza-payne rearrangement and intramolecular cyclization Organic Letters. 4: 115-117. DOI: 10.1021/ol0169877  0.752
2002 Bui VP, Hudlicky T, Hansen TV, Stenstrom Y. Direct biooxidation of arenes to corresponding catechols with E. coli JM109 (pDTG602). Application to synthesis of combretastatins A-1 and B-1 Tetrahedron Letters. 43: 2839-2841. DOI: 10.1016/S0040-4039(02)00389-1  0.716
2001 Guo Z, Sanghvi YS, Brammer LE, Hudlicky T. Synthesis of 2',3'-dideoxy-2',3'-didehydro nucleosides via a serendipitous route. Nucleosides, Nucleotides & Nucleic Acids. 20: 1263-6. PMID 11562999 DOI: 10.1081/Ncn-100002532  0.477
2001 Tullis JS, Laufersweiler MJ, VanRens JC, Natchus MG, Bookland RG, Almstead NG, Pikul S, De B, Hsieh LC, Janusz MJ, Branch TM, Peng SX, Jin YY, Hudlicky T, Oppong K. The development of new carboxylic acid-based MMP inhibitors derived from a cyclohexylglycine scaffold. Bioorganic & Medicinal Chemistry Letters. 11: 1975-9. PMID 11454461 DOI: 10.1016/S0960-894X(01)00371-7  0.671
2001 Hudlicky T, Oppong K, Duan C, Stanton C, Laufersweiler MJ, Natchus MG. Chemoenzymatic synthesis of functionalized cyclohexylglycines and alpha-methylcyclohexylglycines via Kazmaier-Claisen rearrangement. Bioorganic & Medicinal Chemistry Letters. 11: 627-9. PMID 11266157 DOI: 10.1016/S0960-894X(01)00013-0  0.711
2001 Schilling S, Rinner U, Chan C, Ghiviriga I, Hudlicky T. Structure assignment of aminoconduritols by 15N NMR correlation spectroscopy; synthesis of a positional isomer of 7-deoxypancratistatin Canadian Journal of Chemistry. 79: 1659-1667. DOI: 10.1139/Cjc-79-11-1659  0.769
2001 Paul BJ, Martinot TA, Willis J, Hudlicky T. Novel O- and N-linked inositol oligomers: A new class of unnatural saccharide mimics Synthesis. 952-956. DOI: 10.1055/S-2001-13397  0.763
2001 Bui VP, Hansen TV, Stenstrøm Y, Hudlicky T, Ribbons DW. A study of substrate specificity of toluene dioxygenase in processing aromatic compounds containing benzylic and/or remote chiral centers New Journal of Chemistry. 25: 116-124. DOI: 10.1039/B006545P  0.734
2001 Paul BJ, Hobbs E, Buccino P, Hudlicky T. Opening of a vinyl aziridine with p-toluenesulfonamide under TBAF catalysis: Synthesis of 3,4-diamino-3,4-dideoxy-L-chiro-inositol Tetrahedron Letters. 42: 6433-6435. DOI: 10.1016/S0040-4039(01)01298-9  0.599
2001 Solis-Oba A, Hudlicky T, Koroniak L, Frey D. Selective electrochemical reduction of cinnamyl ethers in the presence of other allylic C-O bonds Tetrahedron Letters. 42: 1241-1243. DOI: 10.1016/S0040-4039(00)02250-4  0.326
2000 Hudlicky T, Restrepo-Sánchez N, Kary PD, Jaramillo-Gómez LM. A short, stereoselective synthesis of neo-inositol. Carbohydrate Research. 324: 200-3. PMID 10724534 DOI: 10.1016/S0008-6215(99)00289-X  0.392
2000 Novak BH, Hudlicky T, Reed JW, Mulzer J, Trauner D. Morphine synthesis and biosynthesis - An update Current Organic Chemistry. 4: 343-362. DOI: 10.2174/1385272003376292  0.792
2000 Bui VP, Hansen TV, Stenstrøm Y, Hudlicky T. Direct biocatalytic synthesis of functionalized catechols: A green alternative to traditional methods with high effective mass yield Green Chemistry. 2: 263-265. DOI: 10.1039/B006988O  0.721
2000 Bui V, Hansen TV, Stenslrom Y, Ribbons DW, Hudlicky T. Toluene dioxygenase-mediated oxidation of aromatic substrates with remote chiral centers Journal of the Chemical Society, Perkin Transactions 1. 1669-1672. DOI: 10.1039/B002143L  0.709
2000 Hudlicky T, Duan C, Reed JW, Yan F, Hudlicky M, Endoma MA, Eger EI. Practical preparation of potentially anesthetic fluorinated ethyl methyl ethers by means of bromine trifluoride and other methods Journal of Fluorine Chemistry. 102: 363-367. DOI: 10.1016/S0022-1139(99)00302-4  0.598
1999 Hudlicky T, Claeboe CD, Brammer LE, Koroniak L, Butora G, Ghiviriga I. Use of Electrochemical Methods as an Alternative to Tin Reagents for the Reduction of Vinyl Halides in Inositol Synthons. The Journal of Organic Chemistry. 64: 4909-4913. PMID 11674569 DOI: 10.1021/Jo990382V  0.377
1999 Reddy GD, Wiest O, Hudlicky T, Schapiro V, Gonzalez D. Electron Transfer Catalyzed [2 + 2] Cycloreversion of Benzene Dimers. The Journal of Organic Chemistry. 64: 2860-2863. PMID 11674357 DOI: 10.1021/Jo982398B  0.455
1999 Cheng M, De B, Almstead NG, Pikul S, Dowty ME, Dietsch CR, Dunaway CM, Gu F, Hsieh LC, Janusz MJ, Taiwo YO, Natchus MG, Hudlicky T, Mandel M. Design, synthesis, and biological evaluation of matrix metalloproteinase inhibitors derived from a modified proline scaffold. Journal of Medicinal Chemistry. 42: 5426-36. PMID 10639284 DOI: 10.1021/Jm9904699  0.35
1999 Koblin DD, Laster MJ, Ionescu P, Gong D, Eger EI, Halsey MJ, Hudlicky T. Polyhalogenated methyl ethyl ethers: solubilities and anesthetic properties. Anesthesia and Analgesia. 88: 1161-7. PMID 10320188 DOI: 10.1097/00000539-199905000-00036  0.309
1999 Hudlicky T, Frey DA, Koroniak L, Claeboe CD, Brammer Jr. LE. Toward a ‘reagent-free’ synthesis Green Chemistry. 1: 57-59. DOI: 10.1039/A901397K  0.372
1999 Hudlicky T, Frey DA, Koroniak L, Claeboe CD, Brammer Jr. LE. Toward a ‘reagent-free’ synthesis Green Chemistry. 1: 57-59. DOI: 10.1039/A901397K  0.372
1999 Hudlicky T, Frey DA, Koroniak L, Claeboe CD, Brammer Jr. LE. Toward a ‘reagent-free’ synthesis Green Chemistry. 1: 57-59. DOI: 10.1039/A901397K  0.372
1999 Hudlicky T, Frey DA, Koroniak L, Claeboe CD, Brammer Jr. LE. Toward a ‘reagent-free’ synthesis Green Chemistry. 1: 57-59. DOI: 10.1039/A901397K  0.372
1999 Desjardins M, Lallemand MC, Freeman S, Hudlicky T, Abboudf K. Synthesis, and biological evaluation of conduritol, and conduramine analogs Journal of the Chemical Society - Perkin Transactions 1. 621-628. DOI: 10.1039/A808329K  0.649
1999 Frey DA, Duan C, Hudlicky T. Model study for a general approach to morphine and noroxymorphone via a rare heck cyclization Organic Letters. 1: 2085-2087. DOI: 10.1021/Ol991135G  0.333
1999 Novak BH, Hudlicky T. New arene cis-dihydrodiol metabolites from β-bromostyrenes Tetrahedron Asymmetry. 10: 2067-2069. DOI: 10.1016/S0957-4166(99)00237-2  0.775
1999 Akgün H, Hudlicky T. Total syntheses of ent-conduramine A and ent-7-deoxypancratistatin Tetrahedron Letters. 40: 3081-3084. DOI: 10.1016/S0040-4039(99)00434-7  0.456
1999 Gonzalez D, Martinot T, Hudlicky T. A short chemoenzymatic synthesis of (+)-narciclasine Tetrahedron Letters. 40: 3077-3080. DOI: 10.1016/S0040-4039(99)00433-5  0.808
1999 Oppong KA, Hudlicky T, Yan F, York C, Nguyen BV. Chemoenzymatic enantiodivergent synthesis of 1,2-dideoxy-2-amino-1- fluoro-allo-inositol Tetrahedron. 55: 2875-2880. DOI: 10.1016/S0040-4020(99)00080-0  0.751
1999 Ghiviriga I, Bottari PQ, Hudlicky T. Elucidation of the stereochemistry of octahydroisoquinoline derivatives by NMR spectroscopy Magnetic Resonance in Chemistry. 37: 653-661. DOI: 10.1002/(Sici)1097-458X(199909)37:9<653::Aid-Mrc511>3.0.Co;2-W  0.346
1999 Hudlicky T, Gonzalez D, Gibson DT. Enzymatic dihydroxylation of aromatics in enantioselective synthesis: Expanding asymmetric methodology Aldrichimica Acta. 32: 35-62.  0.58
1999 Hudlicky T. Asymmetric Synthesis: Preface Current Organic Chemistry. 3: x.  0.378
1998 Nugent TC, Hudlicky T. Chemoenzymatic Synthesis of All Four Stereoisomers of Sphingosine from Chlorobenzene: Glycosphingolipid Precursors(1)(a). The Journal of Organic Chemistry. 63: 510-520. PMID 11672039 DOI: 10.1021/Jo971335A  0.346
1998 Hudlicky T. Natural product synthesis via biocatalysis: An essay on the merits of multidisciplinary ventures Journal of the Brazilian Chemical Society. 9: 313-318. DOI: 10.1590/S0103-50531998000400003  0.369
1998 Butora G, Gum AG, Hudlicky T, Abboud KA. Advanced intramolecular diels-alder study toward the synthesis of (-)- morphine: Structure correction of a previously reported Diels-Alder product Synthesis. 275-278. DOI: 10.1055/S-1998-4529  0.376
1998 Brammer LE, Hudlicky T. Inositol synthesis: Concise preparation of L-chiro-inositol and muco- inositol from a common intermediate Tetrahedron Asymmetry. 9: 2011-2014. DOI: 10.1016/S0957-4166(98)00182-7  0.337
1998 Jalil Miah MA, Hudlicky T, Reed JW. Chapter 2 Cephalotaxus Alkaloids Alkaloids: Chemistry and Biology. 51: 199-269. DOI: 10.1016/S0099-9598(08)60006-1  0.538
1998 Hudlicky T, Gonzalez D, Stabile M, Endoma MAA, Deluca M, Parker D, Gibson DT, Resnick SM, Whited GM. New metabolites from the microbial oxidation of fluorinated aromatic compounds Journal of Fluorine Chemistry. 89: 23-30. DOI: 10.1016/S0022-1139(98)00081-5  0.485
1997 Desjardins M, Lallemand MC, Hudlicky T, Abboud KA. Polyhydroxylated Tetrahydronaphthalene Ethers: Synthesis and Molecular Properties Synlett. 1997: 728-730. DOI: 10.1055/S-1997-3254  0.385
1997 Banwell MG, Haddad N, Hudlicky T, Nugent TC, Mackay MF, Richards SL. Regio- and stereo-chemical outcomes in the nucleophilic ring cleavage reactions of mono-epoxides derived from cis-1,2-dihydrocatechols Journal of the Chemical Society - Perkin Transactions 1. 1779-1791. DOI: 10.1039/A700733G  0.405
1997 Gonzalez D, Schapiro V, Seoane G, Hudlicky T, Abboud K. Chemoenzymatic synthesis of unnatural amino acids via modified Claisen rearrangement of glycine enolates. Approach to morphine synthesis Journal of Organic Chemistry. 62: 1194-1195. DOI: 10.1021/Jo962315W  0.721
1997 Butora G, Reed JW, Hudlicky T, Brammer LE, Higgs PI, Simmons DP, Heard NE. Electrochemical versus anionic oxygenation of azathymine derivatives Journal of the American Chemical Society. 119: 7694-7701. DOI: 10.1021/Ja9711122  0.531
1997 Gonzalez D, Schapiro V, Seoane G, Hudlicky T. New metabolites from toluene dioxygenase dihydroxylation of oxygenated biphenyls Tetrahedron Asymmetry. 8: 975-977. DOI: 10.1016/S0957-4166(97)00059-1  0.673
1997 Endoma MA, Butora G, Claeboe CD, Hudlicky T, Abboud KA. Chemoenzymatic and electrochemical oxidations in the synthesis of octahydroisoquindines for conversion to morphine. Relative merits of radical vs. acid-catalyzed cyclizations Tetrahedron Letters. 38: 8833-8836. DOI: 10.1016/S0040-4039(97)10384-7  0.461
1997 Lallemand MC, Desjardins M, Freeman S, Hudlicky T. Synthesis of conduritol, conduramine, and validoxylamine analogs from tetrahydronaphthalene-cis-diol Tetrahedron Letters. 38: 7693-7696. DOI: 10.1016/S0040-4039(97)10008-9  0.634
1997 Nguyen BV, York C, Hudlicky T. Chemoenzymatic synthesis of deoxyfluoroinositols: 5-deoxy-5-fluoro-myo- inositol and 3-deoxy-3-fluoro-L-chiro-inositol Tetrahedron. 53: 8807-8814. DOI: 10.1016/S0040-4020(97)90392-6  0.411
1997 Yan F, Nguyen BV, York C, Hudlicky T. Chemoenzymatic synthesis of fluorinated carbohydrates: 2-deoxy-2-fluoro-D-glucose and 5-deoxy-5-fluoro-manno-γ-lactol Tetrahedron. 53: 11541-11548. DOI: 10.1016/S0040-4020(97)00746-1  0.392
1997 Desjardins M, Brammer LE, Hudlicky T. A practical multigram-scale synthesis of allo-inositol Carbohydrate Research. 304: 39-42. DOI: 10.1016/S0008-6215(97)00186-9  0.372
1996 Hudlicky T, Entwistle DA, Pitzer KK, Thorpe AJ. Modern Methods of Monosaccharide Synthesis from Non-Carbohydrate Sources. Chemical Reviews. 96: 1195-1220. PMID 11848785 DOI: 10.1021/Cr9403300  0.333
1996 Hudlicky T, Abboud KA, Entwistle DA, Fan R, Maurya R, Thorpe AJ, Bolonick J, Myers B. Toluene-dioxygenase-mediated cis-dihydroxylation of aromatics in enantioselective synthesis. Iterative glycoconjugate coupling strategy and combinatorial design for the synthesis of oligomers of nor-saccharides, inositols and pseudosugars with interesting molecular porperties Synthesis. 897-911. DOI: 10.1055/S-1996-4440  0.428
1996 Hudlicky T, Endoma MAA, Butora G. Nucleophilic substitution of protected β-bromoethyl cyclohexadiene-cis-diol as an alternative to direct microbial oxidation of β-functionalized phenethyl substrates Journal of the Chemical Society - Perkin Transactions 1. 2187-2192. DOI: 10.1039/P19960002187  0.406
1996 Hudlicky T, Thorpe AJ. Current status and future perspectives of cyclohexadiene-cis-diols in organic synthesis: Versatile intermediates in the concise design of natural products Chemical Communications. 1993-2000. DOI: 10.1039/Cc9960001993  0.36
1996 Hudlicky T, Tian X, Königsberger K, Maurya R, Rouden J, Fan B. Toluene dioxygenase-mediated cis-dihydroxylation of aromatics in enantioselective synthesis. Asymmetric total syntheses of pancratistatin and 7-deoxypancratistatin, promising antitumor agents Journal of the American Chemical Society. 118: 10752-10765. DOI: 10.1021/Ja960596J  0.452
1996 Hudlicky T, Endoma MAA, Butora G. New chiral synthons from the microbial oxidation of bromonaphthalenes Tetrahedron Asymmetry. 7: 61-68. DOI: 10.1016/0957-4166(95)00421-1  0.317
1996 Butora G, Hudlicky T, Fearnley SP, Gum AG, Stabile MR, Abboud K. Chemoenzymatic synthesis of the morphine skeleton via radical cyclization and a C10-C11 closure Tetrahedron Letters. 37: 8155-8158. DOI: 10.1016/0040-4039(96)01867-9  0.411
1995 Tian X, Maurya R, Königsberger K, Hudlicky T. Asymmetric Total Synthesis of (+)-7-Deoxypancratistatin Synlett. 1995: 1125-1126. DOI: 10.1055/S-1995-5221  0.473
1995 Tian X, Maurya R, Königsberger K, Hudlicky T. Asymmetric Total Synthesis of (+)-7-Deoxypancratistatin Synlett. 1995: 1125-1126. DOI: 10.1055/s-1995-5221  0.369
1995 Tian X, Maurya R, Königsberger K, Hudlicky T. Asymmetric Total Synthesis of (+)-7-Deoxypancratistatin Synlett. 1995: 1125-1126. DOI: 10.1055/s-1995-5221  0.369
1995 Tian X, Maurya R, Königsberger K, Hudlicky T. Asymmetric Total Synthesis of (+)-7-Deoxypancratistatin Synlett. 1995: 1125-1126. DOI: 10.1055/s-1995-5221  0.369
1995 Tian X, Maurya R, Königsberger K, Hudlicky T. Asymmetric Total Synthesis of (+)-7-Deoxypancratistatin Synlett. 1995: 1125-1126. DOI: 10.1055/s-1995-5221  0.369
1995 McKibben BP, Barnosky GS, Hudlicky T. Unusual Dehalogenation of a Bridgehead Halide. Biocatalytic Conversion of Halocyclohexadiene-cis-diols to the trans-Isomers and Synthesis of Optically Pure Cyclohexadiene-trans-diols Synlett. 1995: 806-808. DOI: 10.1055/S-1995-5099  0.359
1995 Hudlicky T, Butora G, Fearnley SP, Gum AG, Persichini PJ, Stabile MR, Merola JS. Intramolecular Diels-Alder reactions of the furan diene (IMDAF); rapid construction of highly functionalised isoquinoline skeletons Journal of the Chemical Society, Perkin Transactions 1. 2393-2398. DOI: 10.1039/P19950002393  0.455
1995 Tian X, Hudlicky T, Königsberger K. First enantioselective total synthesis of (+)-pancratistatin: An unusual set of problems Journal of the American Chemical Society. 117: 3643-3644. DOI: 10.1021/Ja00117A046  0.345
1995 Stabile MR, Hudlicky T, Meisels ML. New chiral synthon from bromoethylbenzene: Absolute stereochemistry of a biooxidation metabolite Tetrahedron: Asymmetry. 6: 537-542. DOI: 10.1016/0957-4166(95)00037-P  0.327
1995 Entwistle DA, Hudlicky T. Synthesis of pseudosugars from microbial metabolites Tetrahedron Letters. 36: 2591-2594. DOI: 10.1016/0040-4039(95)00347-F  0.317
1995 Stabile MR, Hudlicky T, Meisels ML, Butora G, Gum AG, Fearnley SP, Thorpe AJ, Ellis MR. Oxidation of 2-(2-bromoethyl)bromobenzene with toluene dioxygenase: Isolation and identification of new chiral synthons Chirality. 7: 556-559. DOI: 10.1002/Chir.530070710  0.32
1994 Hudlicky T, Rouden J, Luna H, Allen S. Microbial oxidation of aromatics in enantiocontrolled synthesis. 2. Rational design of aza sugars (endo-nitrogenous). Total synthesis of +-kifunensine, mannojirimycin, and other glycosidase inhibitors. Journal of the American Chemical Society. 116: 5099-107. PMID 20000784 DOI: 10.1021/Ja00091A011  0.503
1994 Whited GM, Downie JC, Hudlicky T, Fearnley SP, Dudding TC, Olivo HF, Parker D. Oxidation of 2-methoxynaphthalene by toluene, naphthalene and biphenyl dioxygenases:structure and absolute stereochemistry of metabolites. Bioorganic & Medicinal Chemistry. 2: 727-34. PMID 7858982 DOI: 10.1016/0968-0896(94)85024-0  0.654
1994 Hudlicky T. Enantioselective synthesis of alkaloids and carbohydrates via chemoenzymatic methods Pure and Applied Chemistry. 66: 2067-2070. DOI: 10.1351/Pac199466102067  0.39
1994 Hudlicky T, Thorpe AJ. Glycoconjugate Coupling Strategy: Synthesis of a L-chiro-Inositol-gala-Quercitol Conjugate and the Synthesis of (+)-proto-Quercitol Synlett. 1994: 899-901. DOI: 10.1055/S-1994-23041  0.401
1994 Hudlicky T, Mandel M, Rouden J, Lee RS, Bachmann B, Dudding T, Yost KJ, Merola JS. Microbial oxidation of aromatics in enantiocontrolled synthesis. Part 1. Expedient and general asymmetric synthesis of inositols and carbohydrates via an unusual oxidation of a polarized diene with potassium permanganate Journal of the Chemical Society, Perkin Transactions 1. 1553-1567. DOI: 10.1039/P19940001553  0.43
1994 Hudlicky T, McKibben BP. New cycloaddition chemistry of 1-chloro-5,6-cis-isopropylidenedioxycyclohexa-1,3-diene derived from the oxidation of halogenobenzenes by Pseudomonas putida 39D Journal of the Chemical Society, Perkin Transactions 1. 485-486. DOI: 10.1039/P19940000485  0.374
1994 Hudlicky T, Nugent T, Griffith W. Chemoenzymic Synthesis of D-erythro- and L-threo-C18-Sphingosines The Journal of Organic Chemistry. 59: 7944-7946. DOI: 10.1021/Jo00105A002  0.307
1994 Hudlicky T, Tian X, Königsberger K, Rouden J. Oxa- and azabicyclo[4.1.0]heptenes as new synthons for C-disaccharide and alkaloid synthesis. Reactivity trends with carbon nucleophiles Journal of Organic Chemistry. 59: 4037-4039. DOI: 10.1021/Jo00094A005  0.383
1994 Hudlicky T, Olivo HF, McKibben B. Microbial oxidation of aromatics in enantiocontrolled synthesis. 3.1 design of amino cyclitols (exo-nitrogenous) and total synthesis of (+)-lycoricidine via acylnitrosyl cycloaddition to polarized 1-halo-1,3-cyclohexadienes Journal of the American Chemical Society. 116: 5108-5115. DOI: 10.1021/Ja00091A012  0.693
1994 Hudlicky T, Rouden J, Luna H, Allen S. Microbial oxidation of aromatics in enantiocontrolled synthesis. 2.1 rational design of aza sugars (endo-nitrogenous). Total synthesis of (+)-kifunensine, mannojirimycin, and other glycosidase inhibitors Journal of the American Chemical Society. 116: 5099-5107.  0.32
1993 Mandel M, Hudlicky T. Conduritol-halo Epoxides: Versatile Synthons for Cyclitol Synthesis Synlett. 1993: 418-420. DOI: 10.1055/s-1993-22478  0.388
1993 Mandel M, Hudlicky T. Conduritol-halo Epoxides: Versatile Synthons for Cyclitol Synthesis Synlett. 1993: 418-420. DOI: 10.1055/s-1993-22478  0.388
1993 Mandel M, Hudlicky T. Conduritol-halo Epoxides: Versatile Synthons for Cyclitol Synthesis Synlett. 1993: 418-420. DOI: 10.1055/s-1993-22478  0.388
1993 Mandel M, Hudlicky T. Conduritol-halo Epoxides: Versatile Synthons for Cyclitol Synthesis Synlett. 1993: 418-420. DOI: 10.1055/s-1993-22478  0.388
1993 Mandel M, Hudlicky T. Conduritol-halo Epoxides: Versatile Synthons for Cyclitol Synthesis Synlett. 1993: 418-420. DOI: 10.1055/s-1993-22478  0.388
1993 Mandel M, Hudlicky T. Conduritol-halo Epoxides: Versatile Synthons for Cyclitol Synthesis Synlett. 1993: 418-420. DOI: 10.1055/S-1993-22478  0.489
1993 Mandel M, Hudlicky T. Conduritol-halo Epoxides: Versatile Synthons for Cyclitol Synthesis Synlett. 1993: 418-420. DOI: 10.1055/s-1993-22478  0.388
1993 Mandel M, Hudlicky T. Conduritol-halo Epoxides: Versatile Synthons for Cyclitol Synthesis Synlett. 1993: 418-420. DOI: 10.1055/s-1993-22478  0.388
1993 Rouden J, Hudlicky T. Total synthesis of (+)-kifunensine, a potent glycosidase inhibitor Journal of the Chemical Society, Perkin Transactions 1. 1095-1997. DOI: 10.1039/P19930001095  0.362
1993 Mandel M, Hudlicky T. General synthesis of inositols by hydrolysis of conduritol epoxides obtained biocatalytically from halogenobenzenes: (+)-D-chiro-lnositol, allo-lnositol, muco-inositol and neo-lnositol Journal of the Chemical Society, Perkin Transactions 1. 741-743. DOI: 10.1039/P19930000741  0.419
1993 Hudlicky T, Rouden J, Luna H. Rational design of aza sugars via biocatalysis: Mannojirimycin and other glycosidase inhibitors Journal of Organic Chemistry. 58: 985-987. DOI: 10.1021/Jo00057A001  0.323
1993 Hudlicky T, Boros EE, Boros CH. New diol metabolites derived by biooxidation of chlorostyrenes with Pseudomonas putida: Determination of absolute stereochemistry and enantiomeric excess by convergent syntheses Tetrahedron: Asymmetry. 4: 1365-1386. DOI: 10.1016/S0957-4166(00)80247-5  0.401
1993 Hudlicky T, Boros CH. New diels-alder dimers of (1S,2R)-cis-1,2-Isopropylidene-dioxy-3-ethenylcyclohexa-3,5-diene Tetrahedron Letters. 34: 2557-2560. DOI: 10.1016/S0040-4039(00)77624-6  0.352
1992 Hudlicky T, Fan R, Luna H, Olivo H, Price J. Enzymatic hydroxylation of arene and symmetry considerations in efficient synthetic design of oxygenated natural products Pure and Applied Chemistry. 64: 1109-1113. DOI: 10.1351/Pac199264081109  0.615
1992 Hudlicky T, Natchus MG, Nugent TC. Improved Practical Synthesis of a Prostaglandin and Carbocyclic Nucleoside Synthon Synthetic Communications. 22: 151-157. DOI: 10.1080/00397919208021086  0.417
1992 Hudlicky T, Boros CH, Boros EE. A Model Study Directed Towards a Practical Enantioselective Total Synthesis of (-)-Morphine Synthesis. 1992: 174-178. DOI: 10.1055/S-1992-34161  0.445
1992 Hudlicky T, Boros EE, Boros CH. Microbial Oxidation ofo-Chlorostyrene: Determination of Absolute Stereochemistry of the cis-Diol Metabolite by a Convergent Synthesis Utilizing an Intramolecular Diels-Alder Reaction Synlett. 1992: 391-393. DOI: 10.1055/S-1992-21355  0.305
1992 Hudlicky T, Boros EE, Boros CH. Microbial Oxidation ofo-Chlorostyrene: Determination of Absolute Stereochemistry of the cis-Diol Metabolite by a Convergent Synthesis Utilizing an Intramolecular Diels-Alder Reaction Synlett. 1992: 391-393. DOI: 10.1055/S-1992-21355  0.305
1992 Hudlicky T, Boros EE, Boros CH. Microbial Oxidation ofo-Chlorostyrene: Determination of Absolute Stereochemistry of the cis-Diol Metabolite by a Convergent Synthesis Utilizing an Intramolecular Diels-Alder Reaction Synlett. 1992: 391-393. DOI: 10.1055/s-1992-21355  0.305
1992 Hudlicky T, Boros EE, Boros CH. Microbial Oxidation ofo-Chlorostyrene: Determination of Absolute Stereochemistry of the cis-Diol Metabolite by a Convergent Synthesis Utilizing an Intramolecular Diels-Alder Reaction Synlett. 1992: 391-393. DOI: 10.1055/s-1992-21355  0.305
1992 Hudlicky T, Boros EE, Boros CH. Microbial Oxidation ofo-Chlorostyrene: Determination of Absolute Stereochemistry of the cis-Diol Metabolite by a Convergent Synthesis Utilizing an Intramolecular Diels-Alder Reaction Synlett. 1992: 391-393. DOI: 10.1055/s-1992-21355  0.305
1992 Hudlicky T, Boros EE, Boros CH. Microbial Oxidation ofo-Chlorostyrene: Determination of Absolute Stereochemistry of the cis-Diol Metabolite by a Convergent Synthesis Utilizing an Intramolecular Diels-Alder Reaction Synlett. 1992: 391-393. DOI: 10.1055/s-1992-21355  0.305
1992 Hudlicky T, Boros EE, Boros CH. Microbial Oxidation ofo-Chlorostyrene: Determination of Absolute Stereochemistry of the cis-Diol Metabolite by a Convergent Synthesis Utilizing an Intramolecular Diels-Alder Reaction Synlett. 1992: 391-393. DOI: 10.1055/s-1992-21355  0.305
1992 Hudlicky T, Boros EE, Boros CH. Microbial Oxidation ofo-Chlorostyrene: Determination of Absolute Stereochemistry of the cis-Diol Metabolite by a Convergent Synthesis Utilizing an Intramolecular Diels-Alder Reaction Synlett. 1992: 391-393. DOI: 10.1055/s-1992-21355  0.305
1992 Hudlicky T, Natchus M. Chemoenzymic enantiocontrolled synthesis of (-)-specionin The Journal of Organic Chemistry. 57: 4740-4746. DOI: 10.1021/Jo00043A037  0.408
1992 Hudlicky T, Olivo HF. A short synthesis of (+)-lycoricidine Journal of the American Chemical Society. 114: 9694-9696. DOI: 10.1021/Ja00050A079  0.701
1992 Hudlicky T, Olivo HF. A short synthesis of (+)-lycoricidine Journal of the American Chemical Society. 114: 9694-9696. DOI: 10.1021/ja00050a079  0.328
1992 Hudlicky T, Olivo HF. A short synthesis of (+)-lycoricidine Journal of the American Chemical Society. 114: 9694-9696. DOI: 10.1021/ja00050a079  0.328
1992 Hudlicky T, Olivo HF. A short synthesis of (+)-lycoricidine Journal of the American Chemical Society. 114: 9694-9696. DOI: 10.1021/ja00050a079  0.328
1992 Hudlicky T, Olivo HF. A short synthesis of (+)-lycoricidine Journal of the American Chemical Society. 114: 9694-9696. DOI: 10.1021/ja00050a079  0.328
1992 Hudlicky T, Olivo HF. A short synthesis of (+)-lycoricidine Journal of the American Chemical Society. 114: 9694-9696. DOI: 10.1021/ja00050a079  0.328
1992 Hudlicky T, Olivo HF. A short synthesis of (+)-lycoricidine Journal of the American Chemical Society. 114: 9694-9696. DOI: 10.1021/ja00050a079  0.328
1992 Hudlicky T, Olivo HF. A short synthesis of (+)-lycoricidine Journal of the American Chemical Society. 114: 9694-9696. DOI: 10.1021/ja00050a079  0.328
1992 Hudlicky T, Gillman G, Andersen C. Homochiral amine synthesis by baker's yeast resolution of a β-keto amide: 1-Phenylethylamine Tetrahedron: Asymmetry. 3: 281-286. DOI: 10.1016/S0957-4166(00)80207-4  0.338
1992 Hudlicky T, Boros EE. Palladium-catalyzed coupling of terminal alkynes to the free cis-diol metabolite produced from the oxidation of bromobenzene by pseudomonas putida: Synthesis of new homochiral 3-alkynyl cis-cyclohexa-3,5-diene-1,2-diols Tetrahedron: Asymmetry. 3: 217-220. DOI: 10.1016/S0957-4166(00)80194-9  0.373
1992 Hudlicky T, Fan R, Reed JW, Carver DR, Hudlicky M, Eger EI. Practical preparation of some potentially anesthetic fluoroalkanes: regiocontrolled introduction of hydrogen atoms Journal of Fluorine Chemistry. 59: 9-14. DOI: 10.1016/S0022-1139(00)80199-2  0.515
1991 Hudlicky T, Price JD, Olivo HF. Enantiocontrolled Total Synthesis of Conduritols:1(+)-Conduritol E and (-)-Conduritol F Synlett. 1991: 645-646. DOI: 10.1055/S-1991-20826  0.633
1991 Hudlicky T, Price JD, Olivo HF. Enantiocontrolled Total Synthesis of Conduritols:1(+)-Conduritol E and (-)-Conduritol F Synlett. 1991: 645-646. DOI: 10.1055/s-1991-20826  0.599
1991 Hudlicky T, Luna H, Olivo HF, Andersen C, Nugent T, Price JD. Biocatalysis as the strategy of choice in the exhaustive enantiomerically controlled synthesis of conduritols Journal of the Chemical Society-Perkin Transactions 1. 2907-2917. DOI: 10.1039/P19910002907  0.647
1991 Hudlicky T, Barbieri G. A new [2 + 3] annulation for highly functionalized dihydrofurans via carbon-carbon bond formation The Journal of Organic Chemistry. 56: 4598-4600. DOI: 10.1021/Jo00015A006  0.343
1991 Hudlicky T, Olivo HF. Stereospecific synthesis of aminocyclitols via cycloadditions of unsymmetrical, optically pure dienes: conduramine A-1 and dihydroconduramine A-1 Tetrahedron Letters. 32: 6077-6080. DOI: 10.1016/0040-4039(91)80757-W  0.688
1991 Hudlicky T, Olivo HF. Stereospecific synthesis of aminocyclitols via cycloadditions of unsymmetrical, optically pure dienes: conduramine A-1 and dihydroconduramine A-1 Tetrahedron Letters. 32: 6077-6080. DOI: 10.1016/0040-4039(91)80757-W  0.688
1991 Hudlicky T, Rulin F, Tsunoda T, Luna H, Andersen C, Price JD. Biocatalysis as a Rational Approach to Enantiodivergent Synthesis of Highly Oxygenated Compounds: (+)- and (-)-Pinitol and Other Cyclitols Israel Journal of Chemistry. 31: 229-238. DOI: 10.1002/Ijch.199100027  0.413
1990 Hudlicky T, Lovelace TC. Formal Total Synthesis of Ipomeamarone via the [2+3] Dihydrofuran Annulation Synthetic Communications. 20: 1721-1732. DOI: 10.1080/00397919008053095  0.441
1990 Hudlicky T, Lovelace TC. Formal Total Synthesis of Ipomeamarone via the [2+3] Dihydrofuran Annulation Synthetic Communications. 20: 1721-1732. DOI: 10.1080/00397919008053095  0.379
1990 Hudlicky T, Lovelace TC. Formal Total Synthesis of Ipomeamarone via the [2+3] Dihydrofuran Annulation Synthetic Communications. 20: 1721-1732. DOI: 10.1080/00397919008053095  0.379
1990 Hudlicky T, Lovelace TC. Formal Total Synthesis of Ipomeamarone via the [2+3] Dihydrofuran Annulation Synthetic Communications. 20: 1721-1732. DOI: 10.1080/00397919008053095  0.379
1990 Hudlicky T, Lovelace TC. Formal Total Synthesis of Ipomeamarone via the [2+3] Dihydrofuran Annulation Synthetic Communications. 20: 1721-1732. DOI: 10.1080/00397919008053095  0.379
1990 Hudlicky T, Lovelace TC. Formal Total Synthesis of Ipomeamarone via the [2+3] Dihydrofuran Annulation Synthetic Communications. 20: 1721-1732. DOI: 10.1080/00397919008053095  0.379
1990 Hudlicky T, Lovelace TC. Formal Total Synthesis of Ipomeamarone via the [2+3] Dihydrofuran Annulation Synthetic Communications. 20: 1721-1732. DOI: 10.1080/00397919008053095  0.379
1990 Hudlicky T, Lovelace TC. Formal Total Synthesis of Ipomeamarone via the [2+3] Dihydrofuran Annulation Synthetic Communications. 20: 1721-1732. DOI: 10.1080/00397919008053095  0.379
1990 Hudlicky T, Seoane G, Price JD, Gadamasetti KG. An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via [4 + 1]Azide-Diene Annulation Methodology Synlett. 1990: 433-440. DOI: 10.1055/S-1990-34718  0.711
1990 Hudlicky T, Seoane G, Price JD, Gadamasetti KG. An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via [4 + 1]Azide-Diene Annulation Methodology Synlett. 1990: 433-440. DOI: 10.1055/s-1990-34718  0.408
1990 Hudlicky T, Seoane G, Price JD, Gadamasetti KG. An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via [4 + 1]Azide-Diene Annulation Methodology Synlett. 1990: 433-440. DOI: 10.1055/s-1990-34718  0.408
1990 Hudlicky T, Seoane G, Price JD, Gadamasetti KG. An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via [4 + 1]Azide-Diene Annulation Methodology Synlett. 1990: 433-440. DOI: 10.1055/s-1990-34718  0.408
1990 Hudlicky T, Seoane G, Price JD, Gadamasetti KG. An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via [4 + 1]Azide-Diene Annulation Methodology Synlett. 1990: 433-440. DOI: 10.1055/s-1990-34718  0.408
1990 Hudlicky T, Seoane G, Price JD, Gadamasetti KG. An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via [4 + 1]Azide-Diene Annulation Methodology Synlett. 1990: 433-440. DOI: 10.1055/s-1990-34718  0.408
1990 Hudlicky T, Seoane G, Price JD, Gadamasetti KG. An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via [4 + 1]Azide-Diene Annulation Methodology Synlett. 1990: 433-440. DOI: 10.1055/s-1990-34718  0.408
1990 Hudlicky T, Seoane G, Price JD, Gadamasetti KG. An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via [4 + 1]Azide-Diene Annulation Methodology Synlett. 1990: 433-440. DOI: 10.1055/s-1990-34718  0.408
1990 Tsunoda T, Hudlicky T. Practical Synthesis of Vinylcyclopropane Synlett. 1990: 322-322. DOI: 10.1055/S-1990-21077  0.404
1990 Hudlicky T, Price JD. Microbial Oxidation of Chloroaromatics in the Enantioselective Synthesis of Carbohydrates: L-Ribonic γ-Lactone Synlett. 1990: 159-160. DOI: 10.1055/S-1990-21020  0.369
1990 Hudlicky T, Olivo HF, Natchus MG, Umpierrez EF, Pandolfi E, Volonterio C. Synthesis of .beta.-methoxy enones via a new two-carbon extension of carboxylic acids The Journal of Organic Chemistry. 55: 4767-4770. DOI: 10.1021/Jo00302A056  0.644
1990 Hudlicky T, Olivo HF, Natchus MG, Umpierrez EF, Pandolfi E, Volonterio C. Synthesis of .beta.-methoxy enones via a new two-carbon extension of carboxylic acids The Journal of Organic Chemistry. 55: 4767-4770. DOI: 10.1021/jo00302a056  0.611
1990 Hudlicky T, Luna H, Price JD, Rulin F. Microbial oxidation of chloroaromatics in the enantiodivergent synthesis of pyrrolizidine alkaloids: trihydroxyheliotridanes The Journal of Organic Chemistry. 55: 4683-4687. DOI: 10.1021/Jo00302A037  0.47
1990 Hudlicky T, Heard NE, Fleming A. 4-Siloxy-.alpha.-bromocrotonate: a new reagent for [2+3] annulation leading to oxygenated cyclopentenes at low temperatures The Journal of Organic Chemistry. 55: 2570-2572. DOI: 10.1021/Jo00296A004  0.322
1990 Hudlicky T, Price JD, Rulin F, Tsunoda T. Efficient and enantiodivergent synthesis of (+)- and (-)-pinitol Journal of the American Chemical Society. 112: 9439-9440. DOI: 10.1021/Ja00181A081  0.313
1990 Hudlicky T, Price JD, Rulin F, Tsunoda T. Efficient and enantiodivergent synthesis of (+)- and (-)-pinitol Journal of the American Chemical Society. 112: 9439-9440. DOI: 10.1021/ja00181a081  0.313
1990 Hudlicky T, Price JD, Rulin F, Tsunoda T. Efficient and enantiodivergent synthesis of (+)- and (-)-pinitol Journal of the American Chemical Society. 112: 9439-9440. DOI: 10.1021/ja00181a081  0.313
1990 Hudlicky T, Price JD, Rulin F, Tsunoda T. Efficient and enantiodivergent synthesis of (+)- and (-)-pinitol Journal of the American Chemical Society. 112: 9439-9440. DOI: 10.1021/ja00181a081  0.313
1990 Hudlicky T, Price JD, Rulin F, Tsunoda T. Efficient and enantiodivergent synthesis of (+)- and (-)-pinitol Journal of the American Chemical Society. 112: 9439-9440. DOI: 10.1021/Ja00181A081  0.313
1990 Hudlicky T, Price JD, Rulin F, Tsunoda T. Efficient and enantiodivergent synthesis of (+)- and (-)-pinitol Journal of the American Chemical Society. 112: 9439-9440. DOI: 10.1021/ja00181a081  0.313
1990 Hudlicky T, Price JD, Rulin F, Tsunoda T. Efficient and enantiodivergent synthesis of (+)- and (-)-pinitol Journal of the American Chemical Society. 112: 9439-9440. DOI: 10.1021/ja00181a081  0.313
1990 Deluca ME, Hudlicky T. Microbial oxidation of naphthalene derivatives. Absolute configuration of metabolites Tetrahedron Letters. 31: 13-16. DOI: 10.1016/S0040-4039(00)94321-1  0.37
1990 HUDLICKY T, RULIN F, LOVELACE TC, REED JW. ChemInform Abstract: Synthesis of Natural Products Containing Five-Membered Rings. An Evolution of General Methodology Cheminform. 21. DOI: 10.1002/chin.199008362  0.571
1989 Hudlicky T, Maxwell MH. A Michael Alternative to Cyclopentene Annulations Synthetic Communications. 19: 1847-1858. DOI: 10.1080/00397918908052574  0.493
1989 Hudlicky T, Seoane G, Pettus T. Enantioselective synthesis of (-)-zeylena from styrene Journal of Organic Chemistry. 54: 4239-4243. DOI: 10.1021/Jo00278A052  0.757
1989 Hudlicky T, Fleming A, Radesca L. The [2 + 3] and [3 + 4] annulation of enones. Enantiocontrolled total synthesis of (-)-retigeranic acid [Erratum to document cited in CA111(11):97589v] Journal of the American Chemical Society. 111: 9136-9136. DOI: 10.1021/Ja00207A040  0.312
1989 Wong HNC, Hon MY, Tse CW, Yip YC, Tanko J, Hudlicky T. Use of cyclopropanes and their derivatives in organic synthesis Chemical Reviews. 89: 165-198. DOI: 10.1021/Cr00091A005  0.388
1989 Fan R, Hudlicky T. Tin analogs of the vinylogous reformatsky reaction. Regio- and stereochemical considerations Tetrahedron Letters. 30: 5533-5536. DOI: 10.1016/S0040-4039(01)93792-X  0.38
1989 Hudlicky T, Luna H, Price JD, Rulin F. An enantiodivergent approach to D- and L-erythrose via microbial oxidation of chlorobenzene Tetrahedron Letters. 30: 4053-4054. DOI: 10.1016/S0040-4039(00)99319-5  0.371
1989 Hudlicky T, Fleming A, Lovelace T. [2+3] Dihydrofuran annulation via vinyloxiranation of carbonyl compounds Tetrahedron. 45: 3021-3037. DOI: 10.1016/S0040-4020(01)80129-0  0.428
1988 Hudlicky T, Seoane G, Lovelace TC. Intramolecular [4 + 1] pyrroline annulation via azide-diene cycloadditions. 2. Formal stereoselective total syntheses of (.+-.)-platynecine, (.+-.)-hastanecine, (.+-.)-turneforcidine, and (.+-.)-dihydroxyheliotridane The Journal of Organic Chemistry. 53: 2094-2099. DOI: 10.1021/Jo00244A047  0.626
1988 Hudlicky T, Seoane G, Lovelace TC. Intramolecular [4 + 1] pyrroline annulation via azide-diene cycloadditions. 2. Formal stereoselective total syntheses of (.+-.)-platynecine, (.+-.)-hastanecine, (.+-.)-turneforcidine, and (.+-.)-dihydroxyheliotridane The Journal of Organic Chemistry. 53: 2094-2099. DOI: 10.1021/jo00244a047  0.398
1988 Hudlicky T, Seoane G, Lovelace TC. Intramolecular [4 + 1] pyrroline annulation via azide-diene cycloadditions. 2. Formal stereoselective total syntheses of (.+-.)-platynecine, (.+-.)-hastanecine, (.+-.)-turneforcidine, and (.+-.)-dihydroxyheliotridane The Journal of Organic Chemistry. 53: 2094-2099. DOI: 10.1021/jo00244a047  0.398
1988 Hudlicky T, Seoane G, Lovelace TC. Intramolecular [4 + 1] pyrroline annulation via azide-diene cycloadditions. 2. Formal stereoselective total syntheses of (.+-.)-platynecine, (.+-.)-hastanecine, (.+-.)-turneforcidine, and (.+-.)-dihydroxyheliotridane The Journal of Organic Chemistry. 53: 2094-2099. DOI: 10.1021/jo00244a047  0.398
1988 Hudlicky T, Seoane G, Lovelace TC. Intramolecular [4 + 1] pyrroline annulation via azide-diene cycloadditions. 2. Formal stereoselective total syntheses of (.+-.)-platynecine, (.+-.)-hastanecine, (.+-.)-turneforcidine, and (.+-.)-dihydroxyheliotridane The Journal of Organic Chemistry. 53: 2094-2099. DOI: 10.1021/jo00244a047  0.398
1988 Hudlicky T, Seoane G, Lovelace TC. Intramolecular [4 + 1] pyrroline annulation via azide-diene cycloadditions. 2. Formal stereoselective total syntheses of (.+-.)-platynecine, (.+-.)-hastanecine, (.+-.)-turneforcidine, and (.+-.)-dihydroxyheliotridane The Journal of Organic Chemistry. 53: 2094-2099. DOI: 10.1021/jo00244a047  0.398
1988 Hudlicky T, Seoane G, Lovelace TC. Intramolecular [4 + 1] pyrroline annulation via azide-diene cycloadditions. 2. Formal stereoselective total syntheses of (.+-.)-platynecine, (.+-.)-hastanecine, (.+-.)-turneforcidine, and (.+-.)-dihydroxyheliotridane The Journal of Organic Chemistry. 53: 2094-2099. DOI: 10.1021/jo00244a047  0.398
1988 Hudlicky T, Seoane G, Lovelace TC. Intramolecular [4 + 1] pyrroline annulation via azide-diene cycloadditions. 2. Formal stereoselective total syntheses of (.+-.)-platynecine, (.+-.)-hastanecine, (.+-.)-turneforcidine, and (.+-.)-dihydroxyheliotridane The Journal of Organic Chemistry. 53: 2094-2099. DOI: 10.1021/jo00244a047  0.398
1988 Wenkert E, Hudlicky T. Synthesis of eburnamonine and dehydroaspidospermidine The Journal of Organic Chemistry. 53: 1953-1957. DOI: 10.1021/jo00244a020  0.372
1988 Wenkert E, Hudlicky T. Synthesis of eburnamonine and dehydroaspidospermidine The Journal of Organic Chemistry. 53: 1953-1957. DOI: 10.1021/jo00244a020  0.372
1988 Wenkert E, Hudlicky T. Synthesis of eburnamonine and dehydroaspidospermidine The Journal of Organic Chemistry. 53: 1953-1957. DOI: 10.1021/jo00244a020  0.372
1988 Wenkert E, Hudlicky T. Synthesis of eburnamonine and dehydroaspidospermidine The Journal of Organic Chemistry. 53: 1953-1957. DOI: 10.1021/jo00244a020  0.372
1988 Wenkert E, Hudlicky T. Synthesis of eburnamonine and dehydroaspidospermidine The Journal of Organic Chemistry. 53: 1953-1957. DOI: 10.1021/jo00244a020  0.372
1988 Wenkert E, Hudlicky T. Synthesis of eburnamonine and dehydroaspidospermidine The Journal of Organic Chemistry. 53: 1953-1957. DOI: 10.1021/jo00244a020  0.372
1988 Wenkert E, Hudlicky T. Synthesis of eburnamonine and dehydroaspidospermidine The Journal of Organic Chemistry. 53: 1953-1957. DOI: 10.1021/jo00244a020  0.372
1988 Wenkert E, Hudlicky T. Synthesis of eburnamonine and dehydroaspidospermidine The Journal of Organic Chemistry. 53: 1953-1957. DOI: 10.1021/jo00244a020  0.372
1988 Wenkert E, Hudlický T. Synthesis of eburnamonine and dehydroaspidospermidine Journal of Organic Chemistry. 53: 1953-1957. DOI: 10.1021/Jo00244A020  0.635
1988 Hudlicky T, Luna H, Barbieri G, Kwart LD. Enantioselective synthesis through microbial oxidation of arenes. 1. Efficient preparation of terpene and prostanoid synthons Journal of the American Chemical Society. 110: 4735-4741. DOI: 10.1021/Ja00222A035  0.364
1988 Hudlicky T, Luna H, Barbieri G, Kwart LD. Enantioselective synthesis through microbial oxidation of arenes. 1. Efficient preparation of terpene and prostanoid synthons Journal of the American Chemical Society. 110: 4735-4741. DOI: 10.1021/ja00222a035  0.323
1988 Hudlicky T, Luna H, Barbieri G, Kwart LD. Enantioselective synthesis through microbial oxidation of arenes. 1. Efficient preparation of terpene and prostanoid synthons Journal of the American Chemical Society. 110: 4735-4741. DOI: 10.1021/ja00222a035  0.323
1988 Hudlicky T, Luna H, Barbieri G, Kwart LD. Enantioselective synthesis through microbial oxidation of arenes. 1. Efficient preparation of terpene and prostanoid synthons Journal of the American Chemical Society. 110: 4735-4741. DOI: 10.1021/ja00222a035  0.323
1988 Hudlicky T, Luna H, Barbieri G, Kwart LD. Enantioselective synthesis through microbial oxidation of arenes. 1. Efficient preparation of terpene and prostanoid synthons Journal of the American Chemical Society. 110: 4735-4741. DOI: 10.1021/ja00222a035  0.323
1988 Hudlicky T, Radesca-Kwart L, Li L, Bryant T. Short, enantioselective synthesis of (−)-retigeranc acid via [2+3] annulation Tetrahedron Letters. 29: 3283-3286. DOI: 10.1016/0040-4039(88)85141-4  0.433
1988 HUDLICKY T, LUNA H, BARBIERI G, KWART LD. ChemInform Abstract: Enantioselective Synthesis Through Microbial Oxidation of Arenes. Part 1. Efficient Preparation of Terpene and Prostanoid Synthons. Cheminform. 19. DOI: 10.1002/chin.198845325  0.341
1988 HUDLICKY T, LUNA H, BARBIERI G, KWART LD. ChemInform Abstract: Enantioselective Synthesis Through Microbial Oxidation of Arenes. Part 1. Efficient Preparation of Terpene and Prostanoid Synthons. Cheminform. 19. DOI: 10.1002/chin.198845325  0.341
1988 HUDLICKY T, LUNA H, BARBIERI G, KWART LD. ChemInform Abstract: Enantioselective Synthesis Through Microbial Oxidation of Arenes. Part 1. Efficient Preparation of Terpene and Prostanoid Synthons. Cheminform. 19. DOI: 10.1002/chin.198845325  0.341
1988 HUDLICKY T, LUNA H, BARBIERI G, KWART LD. ChemInform Abstract: Enantioselective Synthesis Through Microbial Oxidation of Arenes. Part 1. Efficient Preparation of Terpene and Prostanoid Synthons. Cheminform. 19. DOI: 10.1002/chin.198845325  0.341
1988 HUDLICKY T, LUNA H, BARBIERI G, KWART LD. ChemInform Abstract: Enantioselective Synthesis Through Microbial Oxidation of Arenes. Part 1. Efficient Preparation of Terpene and Prostanoid Synthons. Cheminform. 19. DOI: 10.1002/chin.198845325  0.341
1988 WENKERT E, HUDLICKY T. ChemInform Abstract: Synthesis of Eburnamonine and Dehydroaspidospermidine. Cheminform. 19. DOI: 10.1002/chin.198837323  0.38
1988 WENKERT E, HUDLICKY T. ChemInform Abstract: Synthesis of Eburnamonine and Dehydroaspidospermidine. Cheminform. 19. DOI: 10.1002/chin.198837323  0.38
1988 WENKERT E, HUDLICKY T. ChemInform Abstract: Synthesis of Eburnamonine and Dehydroaspidospermidine. Cheminform. 19. DOI: 10.1002/chin.198837323  0.38
1988 WENKERT E, HUDLICKY T. ChemInform Abstract: Synthesis of Eburnamonine and Dehydroaspidospermidine. Cheminform. 19. DOI: 10.1002/chin.198837323  0.38
1988 WENKERT E, HUDLICKY T. ChemInform Abstract: Synthesis of Eburnamonine and Dehydroaspidospermidine. Cheminform. 19. DOI: 10.1002/chin.198837323  0.38
1988 WENKERT E, HUDLICKY T. ChemInform Abstract: Synthesis of Eburnamonine and Dehydroaspidospermidine. Cheminform. 19. DOI: 10.1002/chin.198837323  0.38
1988 WENKERT E, HUDLICKY T. ChemInform Abstract: Synthesis of Eburnamonine and Dehydroaspidospermidine. Cheminform. 19. DOI: 10.1002/chin.198837323  0.38
1988 HUDLICKY T, SEOANE G, LOVELACE TC. ChemInform Abstract: Intramolecular (4 + 1)Pyrroline Annulation via Azide-Diene Cycloadditions. Part 2. Formal Stereoselective Total Syntheses of (.+-.)-Platynecine, (.+-.)-Hastanecine, (.+-.)-Turneforcidine, and (.+-.)-Dihydroxyheliotridane. Cheminform. 19. DOI: 10.1002/chin.198837320  0.38
1988 HUDLICKY T, SEOANE G, LOVELACE TC. ChemInform Abstract: Intramolecular (4 + 1)Pyrroline Annulation via Azide-Diene Cycloadditions. Part 2. Formal Stereoselective Total Syntheses of (.+-.)-Platynecine, (.+-.)-Hastanecine, (.+-.)-Turneforcidine, and (.+-.)-Dihydroxyheliotridane. Cheminform. 19. DOI: 10.1002/chin.198837320  0.672
1988 HUDLICKY T, SEOANE G, LOVELACE TC. ChemInform Abstract: Intramolecular (4 + 1)Pyrroline Annulation via Azide-Diene Cycloadditions. Part 2. Formal Stereoselective Total Syntheses of (.+-.)-Platynecine, (.+-.)-Hastanecine, (.+-.)-Turneforcidine, and (.+-.)-Dihydroxyheliotridane. Cheminform. 19. DOI: 10.1002/chin.198837320  0.38
1988 HUDLICKY T, SEOANE G, LOVELACE TC. ChemInform Abstract: Intramolecular (4 + 1)Pyrroline Annulation via Azide-Diene Cycloadditions. Part 2. Formal Stereoselective Total Syntheses of (.+-.)-Platynecine, (.+-.)-Hastanecine, (.+-.)-Turneforcidine, and (.+-.)-Dihydroxyheliotridane. Cheminform. 19. DOI: 10.1002/chin.198837320  0.38
1988 HUDLICKY T, SEOANE G, LOVELACE TC. ChemInform Abstract: Intramolecular (4 + 1)Pyrroline Annulation via Azide-Diene Cycloadditions. Part 2. Formal Stereoselective Total Syntheses of (.+-.)-Platynecine, (.+-.)-Hastanecine, (.+-.)-Turneforcidine, and (.+-.)-Dihydroxyheliotridane. Cheminform. 19. DOI: 10.1002/chin.198837320  0.38
1988 HUDLICKY T, NATCHUS MG, SINAI-ZINGDE G. ChemInform Abstract: Stereocontrolled Total Synthesis of Pentalenenes via (2 + 3) and (4 + 1) Cyclopentene Annulation Methodologies. Cheminform. 19. DOI: 10.1002/chin.198811164  0.376
1987 Barbieri G, Seoane G, Trabazo JL, Riva A, Umpierrez F, Radesca L, Tubio R, Kwart LD, Hudlicky T. General method of synthesis for natural long-chain beta-diketones. Journal of Natural Products. 50: 646-9. PMID 3430164 DOI: 10.1021/Np50052A012  0.611
1987 Hudlicky T, Sinai-zingde G, Seoane G. Mild Methodology for [4+1] Pyrroline Annulation. Second Generation Synthesis of Pyrrolizidine Alkaloids Synthetic Communications. 17: 1155-1163. DOI: 10.1080/00397918708063965  0.706
1987 Hudlicky T, Sinai-zingde G, Seoane G. Mild Methodology for [4+1] Pyrroline Annulation. Second Generation Synthesis of Pyrrolizidine Alkaloids Synthetic Communications. 17: 1155-1163. DOI: 10.1080/00397918708063965  0.661
1987 Hudlicky T, Sinai-zingde G, Seoane G. Mild Methodology for [4+1] Pyrroline Annulation. Second Generation Synthesis of Pyrrolizidine Alkaloids Synthetic Communications. 17: 1155-1163. DOI: 10.1080/00397918708063965  0.355
1987 Hudlicky T, Sinai-zingde G, Seoane G. Mild Methodology for [4+1] Pyrroline Annulation. Second Generation Synthesis of Pyrrolizidine Alkaloids Synthetic Communications. 17: 1155-1163. DOI: 10.1080/00397918708063965  0.355
1987 Hudlicky T, Sinai-zingde G, Seoane G. Mild Methodology for [4+1] Pyrroline Annulation. Second Generation Synthesis of Pyrrolizidine Alkaloids Synthetic Communications. 17: 1155-1163. DOI: 10.1080/00397918708063965  0.355
1987 Hudlicky T, Sinai-zingde G, Seoane G. Mild Methodology for [4+1] Pyrroline Annulation. Second Generation Synthesis of Pyrrolizidine Alkaloids Synthetic Communications. 17: 1155-1163. DOI: 10.1080/00397918708063965  0.355
1987 Hudlicky T, Sinai-zingde G, Seoane G. Mild Methodology for [4+1] Pyrroline Annulation. Second Generation Synthesis of Pyrrolizidine Alkaloids Synthetic Communications. 17: 1155-1163. DOI: 10.1080/00397918708063965  0.355
1987 Hudlicky T, Sinai-zingde G, Seoane G. Mild Methodology for [4+1] Pyrroline Annulation. Second Generation Synthesis of Pyrrolizidine Alkaloids Synthetic Communications. 17: 1155-1163. DOI: 10.1080/00397918708063965  0.355
1987 Barbieri G, Seoane G, Trabazo J, Riva A, Umpierrez F, Radesca L, Tubio R, Kwart LD, Hudlicky T. General Method of Synthesis for Natural Long-Chain β/-Diketones Journal of Natural Products. 50: 646-649. DOI: 10.1021/np50052a012  0.564
1987 Hudlicky T, Natchus MG, Sinai-Zingde G. Stereocontrolled total synthesis of pentalenenes via [2 + 3] and [4 + 1] cyclopentene annulation methodologies The Journal of Organic Chemistry. 52: 4641-4644. DOI: 10.1021/Jo00229A051  0.332
1987 Hudlicky T, Natchus MG, Sinai-Zingde G. Stereocontrolled total synthesis of pentalenenes via [2 + 3] and [4 + 1] cyclopentene annulation methodologies The Journal of Organic Chemistry. 52: 4641-4644. DOI: 10.1021/jo00229a051  0.372
1987 Hudlicky T, Natchus MG, Sinai-Zingde G. Stereocontrolled total synthesis of pentalenenes via [2 + 3] and [4 + 1] cyclopentene annulation methodologies The Journal of Organic Chemistry. 52: 4641-4644. DOI: 10.1021/jo00229a051  0.372
1987 Hudlicky T, Natchus MG, Sinai-Zingde G. Stereocontrolled total synthesis of pentalenenes via [2 + 3] and [4 + 1] cyclopentene annulation methodologies The Journal of Organic Chemistry. 52: 4641-4644. DOI: 10.1021/jo00229a051  0.372
1987 Hudlicky T, Natchus MG, Sinai-Zingde G. Stereocontrolled total synthesis of pentalenenes via [2 + 3] and [4 + 1] cyclopentene annulation methodologies The Journal of Organic Chemistry. 52: 4641-4644. DOI: 10.1021/jo00229a051  0.372
1987 Hudlicky T, Radesca L, Rigby HL. Menthyl 2-bromocrotonate and menthyl 4-bromocrotonate: reagents for chiral vinylogous Darzens and Reformatsky reactions The Journal of Organic Chemistry. 52: 4397-4399. DOI: 10.1021/Jo00228A049  0.332
1987 Fleming A, Sinai-Zingde G, Natchus M, Hudlicky T. [2+3] Cyclopentene annulation and other trimethylsilyl iodide-mediated rearrangement pathways of vinylcyclopropanes Tetrahedron Letters. 28: 167-170. DOI: 10.1016/S0040-4039(00)95677-6  0.332
1987 Hudlicky T, Sinai-Zingde G, Natchus M, Ranu B, Papadopolous P. System oriented design of triquinanes: stereocontrolled synthesis of pentalenic acid and pentalenene Tetrahedron. 43: 5685-5721. DOI: 10.1016/S0040-4020(01)87747-4  0.64
1986 Kwart LD, Tiedje M, Frazier JO, Hudlicky T. Total Synthesis of (±)-Epiisocomenes VIA Hydrogenation of “Chatterjee's Ketone” Synthetic Communications. 16: 393-399. DOI: 10.1080/00397918608057714  0.346
1986 Carman L, Kwart LD, Hudlicky T. Claisen/Ozonolysis Alternative to Alkylation of Enolate Anions. Synthesis of 1,4-Dicarbonyl Compounds Synthetic Communications. 16: 169-182. DOI: 10.1080/00397918608057705  0.429
1986 Carman L, Kwart LD, Hudlicky T. Claisen/Ozonolysis Alternative to Alkylation of Enolate Anions. Synthesis of 1,4-Dicarbonyl Compounds Synthetic Communications. 16: 169-182. DOI: 10.1080/00397918608057705  0.335
1986 Carman L, Kwart LD, Hudlicky T. Claisen/Ozonolysis Alternative to Alkylation of Enolate Anions. Synthesis of 1,4-Dicarbonyl Compounds Synthetic Communications. 16: 169-182. DOI: 10.1080/00397918608057705  0.335
1986 Carman L, Kwart LD, Hudlicky T. Claisen/Ozonolysis Alternative to Alkylation of Enolate Anions. Synthesis of 1,4-Dicarbonyl Compounds Synthetic Communications. 16: 169-182. DOI: 10.1080/00397918608057705  0.335
1986 Carman L, Kwart LD, Hudlicky T. Claisen/Ozonolysis Alternative to Alkylation of Enolate Anions. Synthesis of 1,4-Dicarbonyl Compounds Synthetic Communications. 16: 169-182. DOI: 10.1080/00397918608057705  0.335
1986 Carman L, Kwart LD, Hudlicky T. Claisen/Ozonolysis Alternative to Alkylation of Enolate Anions. Synthesis of 1,4-Dicarbonyl Compounds Synthetic Communications. 16: 169-182. DOI: 10.1080/00397918608057705  0.335
1986 Carman L, Kwart LD, Hudlicky T. Claisen/Ozonolysis Alternative to Alkylation of Enolate Anions. Synthesis of 1,4-Dicarbonyl Compounds Synthetic Communications. 16: 169-182. DOI: 10.1080/00397918608057705  0.335
1986 Carman L, Kwart LD, Hudlicky T. Claisen/Ozonolysis Alternative to Alkylation of Enolate Anions. Synthesis of 1,4-Dicarbonyl Compounds Synthetic Communications. 16: 169-182. DOI: 10.1080/00397918608057705  0.335
1986 Hudlicky T, Kwart LD, Tiedje MH, Ranu BC, Short RP, Frazier JO, Rigby HL. General Methodology for the Topologically Selective Preparation of Linear and Nonlinear Tricyclopentanoids of Hirsutane and Isocomene Typeviaa Claisen Rearrangement / Cyclopentene Annulation Sequence. Total Synthesis of (±)- Epiisocomene Synthesis. 1986: 716-727. DOI: 10.1055/S-1986-31756  0.668
1986 Hudlicky T, Radesca L, Luna H, Anderson FE. New vinylcyclopropanation methodology and reagents for potential [2 + 3] cyclopentene, dihydrofuran, and pyrroline annulations The Journal of Organic Chemistry. 51: 4746-4748. DOI: 10.1021/Jo00374A055  0.302
1986 Hudlicky T, Frazier JO, Seoane G, Tiedje M, Seoane A, Kwart LD, Beal C. Topological selectivity in the intramolecular [4 + 1] pyrroline annulation. Formal total stereospecific synthesis of (.+-.)-supinidine, (.+-.)-isoretronecanol, and (.+-.)-trachelanthamidine Journal of the American Chemical Society. 108: 3755-3762. DOI: 10.1021/Ja00273A033  0.674
1986 Hudlicky T, Frazier JO, Seoane G, Tiedje M, Seoane A, Kwart LD, Beal C. Topological selectivity in the intramolecular [4 + 1] pyrroline annulation. Formal total stereospecific synthesis of (.+-.)-supinidine, (.+-.)-isoretronecanol, and (.+-.)-trachelanthamidine Journal of the American Chemical Society. 108: 3755-3762. DOI: 10.1021/ja00273a033  0.321
1986 Hudlicky T, Frazier JO, Seoane G, Tiedje M, Seoane A, Kwart LD, Beal C. Topological selectivity in the intramolecular [4 + 1] pyrroline annulation. Formal total stereospecific synthesis of (.+-.)-supinidine, (.+-.)-isoretronecanol, and (.+-.)-trachelanthamidine Journal of the American Chemical Society. 108: 3755-3762. DOI: 10.1021/ja00273a033  0.321
1986 Hudlicky T, Frazier JO, Seoane G, Tiedje M, Seoane A, Kwart LD, Beal C. Topological selectivity in the intramolecular [4 + 1] pyrroline annulation. Formal total stereospecific synthesis of (.+-.)-supinidine, (.+-.)-isoretronecanol, and (.+-.)-trachelanthamidine Journal of the American Chemical Society. 108: 3755-3762. DOI: 10.1021/ja00273a033  0.321
1986 Hudlicky T, Frazier JO, Seoane G, Tiedje M, Seoane A, Kwart LD, Beal C. Topological selectivity in the intramolecular [4 + 1] pyrroline annulation. Formal total stereospecific synthesis of (.+-.)-supinidine, (.+-.)-isoretronecanol, and (.+-.)-trachelanthamidine Journal of the American Chemical Society. 108: 3755-3762. DOI: 10.1021/ja00273a033  0.321
1986 Hudlicky T, Frazier JO, Seoane G, Tiedje M, Seoane A, Kwart LD, Beal C. Topological selectivity in the intramolecular [4 + 1] pyrroline annulation. Formal total stereospecific synthesis of (.+-.)-supinidine, (.+-.)-isoretronecanol, and (.+-.)-trachelanthamidine Journal of the American Chemical Society. 108: 3755-3762. DOI: 10.1021/ja00273a033  0.321
1986 Hudlicky T, Frazier JO, Seoane G, Tiedje M, Seoane A, Kwart LD, Beal C. Topological selectivity in the intramolecular [4 + 1] pyrroline annulation. Formal total stereospecific synthesis of (.+-.)-supinidine, (.+-.)-isoretronecanol, and (.+-.)-trachelanthamidine Journal of the American Chemical Society. 108: 3755-3762. DOI: 10.1021/ja00273a033  0.321
1986 Hudlicky T, Frazier JO, Seoane G, Tiedje M, Seoane A, Kwart LD, Beal C. Topological selectivity in the intramolecular [4 + 1] pyrroline annulation. Formal total stereospecific synthesis of (.+-.)-supinidine, (.+-.)-isoretronecanol, and (.+-.)-trachelanthamidine Journal of the American Chemical Society. 108: 3755-3762. DOI: 10.1021/ja00273a033  0.321
1986 HUDLICKY T, FRAZIER JO, SEOANE G, TIEDJE M, SEOANE A, KWART LD, BEAL C. ChemInform Abstract: Topological Selectivity in the Intramolecular [4 + 1] Pyrroline Annulation. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198642305  0.602
1986 CARMAN L, KWART LD, HUDLICKY T. ChemInform Abstract: Derivatives Claisen/Ozonolysis Alternative to Alkylation of Enolate Anions. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198630152  0.396
1986 HUDLICKY T, GOVINDAN SV, FRAZIER JO. ChemInform Abstract: Heteroatom Cyclopentene Annulation. Synthesis of Guaiane Ring System. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198610206  0.335
1986 HUDLICKY T, GOVINDAN SV, FRAZIER JO. ChemInform Abstract: Heteroatom Cyclopentene Annulation. Synthesis of Guaiane Ring System. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198610206  0.335
1986 HUDLICKY T, GOVINDAN SV, FRAZIER JO. ChemInform Abstract: Heteroatom Cyclopentene Annulation. Synthesis of Guaiane Ring System. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198610206  0.335
1985 Hudlicky T, Govindan SV, Frazier JO. Heteroatom cyclopentene annulation. Synthesis of guaiane ring system The Journal of Organic Chemistry. 50: 4166-4171. DOI: 10.1021/Jo00221A043  0.432
1985 Hudlicky T, Govindan SV, Frazier JO. Heteroatom cyclopentene annulation. Synthesis of guaiane ring system The Journal of Organic Chemistry. 50: 4166-4171. DOI: 10.1021/jo00221a043  0.319
1985 Hudlicky T, Govindan SV, Frazier JO. Heteroatom cyclopentene annulation. Synthesis of guaiane ring system The Journal of Organic Chemistry. 50: 4166-4171. DOI: 10.1021/jo00221a043  0.319
1985 Hudlicky T, Govindan SV, Frazier JO. Heteroatom cyclopentene annulation. Synthesis of guaiane ring system The Journal of Organic Chemistry. 50: 4166-4171. DOI: 10.1021/jo00221a043  0.319
1985 Hudlicky T, Govindan SV, Frazier JO. Heteroatom cyclopentene annulation. Synthesis of guaiane ring system The Journal of Organic Chemistry. 50: 4166-4171. DOI: 10.1021/jo00221a043  0.319
1985 Hudlicky T, Govindan SV, Frazier JO. Heteroatom cyclopentene annulation. Synthesis of guaiane ring system The Journal of Organic Chemistry. 50: 4166-4171. DOI: 10.1021/jo00221a043  0.319
1985 Hudlicky T, Govindan SV, Frazier JO. Heteroatom cyclopentene annulation. Synthesis of guaiane ring system The Journal of Organic Chemistry. 50: 4166-4171. DOI: 10.1021/jo00221a043  0.319
1985 Hudlicky T, Govindan SV, Frazier JO. Heteroatom cyclopentene annulation. Synthesis of guaiane ring system The Journal of Organic Chemistry. 50: 4166-4171. DOI: 10.1021/jo00221a043  0.319
1985 Hudlicky T, Ranu BC, Naqvi SM, Srnak A. Intramolecular Simmons-Smith reaction and other synthetic alternatives to cyclopropanation of dienic diazo ketones. Parallel decomposition pathways of a sterically congested diazo ketone and its vinylcyclopropane under thermal, photolytic, acid-catalyzed, and radical-release conditions The Journal of Organic Chemistry. 50: 123-127. DOI: 10.1021/Jo00201A026  0.63
1985 Hudlicky T, Frazier JO, Kwart LD. Intramolecular [4 + 1] pyrroline annulation approach to pyrrolizidine alkaloids. Formal total synthesis of (±)-supinidine. Tetrahedron Letters. 26: 3523-3526. DOI: 10.1016/S0040-4039(00)89181-9  0.456
1985 Hudlicky T, Natchus MG, Kwart LD, Colwell BL. Studies in the regioselectivity of the vinylogous Reformatsky reaction with ambident electrophiles: reversibility, mechanism, and synthetic utility The Journal of Organic Chemistry. 50: 4300-4306. DOI: 10.1002/Chin.198621075  0.305
1985 HUDLICKY T, FRAZIER JO, KWART LD. ChemInform Abstract: INTRAMOLECULAR (4 + 1) PYRROLINE ANNULATION APPROACH TO PYRROLIZIDINE ALKALOIDS. FORMAL TOTAL SYNTHESIS OF (.+-.)-SUPINIDINE Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198549191  0.338
1985 HUDLICKY T, FRAZIER JO, KWART LD. ChemInform Abstract: INTRAMOLECULAR (4 + 1) PYRROLINE ANNULATION APPROACH TO PYRROLIZIDINE ALKALOIDS. FORMAL TOTAL SYNTHESIS OF (.+-.)-SUPINIDINE Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198549191  0.338
1985 HUDLICKY T, FRAZIER JO, KWART LD. ChemInform Abstract: INTRAMOLECULAR (4 + 1) PYRROLINE ANNULATION APPROACH TO PYRROLIZIDINE ALKALOIDS. FORMAL TOTAL SYNTHESIS OF (.+-.)-SUPINIDINE Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198549191  0.338
1985 HUDLICKY T, RANU BC, NAQVI SM, SRNAK A. ChemInform Abstract: INTRAMOLECULAR SIMMONS-SMITH REACTION AND OTHER SYNTHETIC ALTERNATIVES TO CYCLOPROPANATION OF DIENIC DIAZO KETONES. PARALLEL DECOMPOSITION PATHWAYS OF A STERICALLY CONGESTED DIAZO KETONE AND ITS VINYLCYCLOPROPANE UNDER THERMAL, PHOTOL Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198522135  0.635
1984 HIRANUMA S, SHIBATA M, HUDLICKY T. ChemInform Abstract: STUDIES IN CEPHALOTAXUS ALKALOIDS. STEREOSPECIFIC TOTAL SYNTHESIS OF HOMOHARRINGTONINE Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198423312  0.382
1984 HIRANUMA S, SHIBATA M, HUDLICKY T. ChemInform Abstract: STUDIES IN CEPHALOTAXUS ALKALOIDS. STEREOSPECIFIC TOTAL SYNTHESIS OF HOMOHARRINGTONINE Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198423312  0.382
1984 HIRANUMA S, SHIBATA M, HUDLICKY T. ChemInform Abstract: STUDIES IN CEPHALOTAXUS ALKALOIDS. STEREOSPECIFIC TOTAL SYNTHESIS OF HOMOHARRINGTONINE Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198423312  0.382
1984 HIRANUMA S, SHIBATA M, HUDLICKY T. ChemInform Abstract: STUDIES IN CEPHALOTAXUS ALKALOIDS. STEREOSPECIFIC TOTAL SYNTHESIS OF HOMOHARRINGTONINE Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198423312  0.382
1984 HIRANUMA S, SHIBATA M, HUDLICKY T. ChemInform Abstract: STUDIES IN CEPHALOTAXUS ALKALOIDS. STEREOSPECIFIC TOTAL SYNTHESIS OF HOMOHARRINGTONINE Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198423312  0.382
1984 HIRANUMA S, SHIBATA M, HUDLICKY T. ChemInform Abstract: STUDIES IN CEPHALOTAXUS ALKALOIDS. STEREOSPECIFIC TOTAL SYNTHESIS OF HOMOHARRINGTONINE Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198423312  0.382
1984 HIRANUMA S, SHIBATA M, HUDLICKY T. ChemInform Abstract: STUDIES IN CEPHALOTAXUS ALKALOIDS. STEREOSPECIFIC TOTAL SYNTHESIS OF HOMOHARRINGTONINE Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198423312  0.382
1984 HIRANUMA S, SHIBATA M, HUDLICKY T. ChemInform Abstract: STUDIES IN CEPHALOTAXUS ALKALOIDS. STEREOSPECIFIC TOTAL SYNTHESIS OF HOMOHARRINGTONINE Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198423312  0.382
1984 SHORT RP, REVOL J, RANU BC, HUDLICKY T. ChemInform Abstract: GENERAL METHOD OF SYNTHESIS OF CYCLOPENTANOID TERPENIC ACIDS. STEREOCONTROLLED TOTAL SYNTHESES OF (.+-.)-ISOCOMENIC ACID AND (.+-.)-EPIISOCOMENIC ACID Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198420288  0.589
1983 Hiranuma S, Shibata M, Hudlicky T. Studies in Cephalotaxus alkaloids. Stereospecific total synthesis of homoharringtonine The Journal of Organic Chemistry. 48: 5321-5326. DOI: 10.1021/jo00174a031  0.378
1983 Hiranuma S, Shibata M, Hudlicky T. Studies in Cephalotaxus alkaloids. Stereospecific total synthesis of homoharringtonine The Journal of Organic Chemistry. 48: 5321-5326. DOI: 10.1021/jo00174a031  0.378
1983 Short RP, Revol JM, Ranu BC, Hudlicky T. General method of synthesis of cyclopentanoid terpenic acids. Stereocontrolled total syntheses of (.+-.)-isocomenic acid and (.+-.)-epiisocomenic acid The Journal of Organic Chemistry. 48: 4453-4461. DOI: 10.1021/Jo00172A003  0.65
1983 Hiranuma S, Shibata M, Hudlicky T. Studies in Cephalotaxus alkaloids. Stereospecific total synthesis of homoharringtonine The Journal of Organic Chemistry. 48: 5321-5326. DOI: 10.1002/Chin.198423312  0.481
1983 Govindan SV, Hudlicky T, Koszyk FJ. Two topologically distinct total syntheses of (.+-.)-sarkomycin The Journal of Organic Chemistry. 48: 3581-3583. DOI: 10.1002/Chin.198412339  0.36
1983 HIRANUMA S, HUDLICKY T. ChemInform Abstract: SYNTHESIS OF HOMOHARRINGTONINE AND ITS DERIVATIVE BY PARTIAL ESTERIFICATION OF CEPHALOTAXINE Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198301348  0.388
1983 HIRANUMA S, HUDLICKY T. ChemInform Abstract: SYNTHESIS OF HOMOHARRINGTONINE AND ITS DERIVATIVE BY PARTIAL ESTERIFICATION OF CEPHALOTAXINE Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198301348  0.388
1983 HIRANUMA S, HUDLICKY T. ChemInform Abstract: SYNTHESIS OF HOMOHARRINGTONINE AND ITS DERIVATIVE BY PARTIAL ESTERIFICATION OF CEPHALOTAXINE Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198301348  0.478
1983 HIRANUMA S, HUDLICKY T. ChemInform Abstract: SYNTHESIS OF HOMOHARRINGTONINE AND ITS DERIVATIVE BY PARTIAL ESTERIFICATION OF CEPHALOTAXINE Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198301348  0.388
1983 HIRANUMA S, HUDLICKY T. ChemInform Abstract: SYNTHESIS OF HOMOHARRINGTONINE AND ITS DERIVATIVE BY PARTIAL ESTERIFICATION OF CEPHALOTAXINE Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198301348  0.388
1983 HIRANUMA S, HUDLICKY T. ChemInform Abstract: SYNTHESIS OF HOMOHARRINGTONINE AND ITS DERIVATIVE BY PARTIAL ESTERIFICATION OF CEPHALOTAXINE Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198301348  0.388
1983 HIRANUMA S, HUDLICKY T. ChemInform Abstract: SYNTHESIS OF HOMOHARRINGTONINE AND ITS DERIVATIVE BY PARTIAL ESTERIFICATION OF CEPHALOTAXINE Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198301348  0.388
1983 HIRANUMA S, HUDLICKY T. ChemInform Abstract: SYNTHESIS OF HOMOHARRINGTONINE AND ITS DERIVATIVE BY PARTIAL ESTERIFICATION OF CEPHALOTAXINE Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198301348  0.388
1982 Hudlicky T, Short RP. Terpenic acids by cyclopentene annulation of exocyclic dienes. Synthesis of the triquinane portion of retigeranic acid The Journal of Organic Chemistry. 47: 1522-1527. DOI: 10.1021/Jo00347A031  0.343
1982 Hiranuma S, Hudlicky T. Synthesis of homoharringtonine and its derivative . Tetrahedron Letters. 23: 3431-3434. DOI: 10.1016/S0040-4039(00)87634-0  0.485
1982 Hiranuma S, Hudlicky T. Synthesis of homoharringtonine and its derivative . Tetrahedron Letters. 23: 3431-3434. DOI: 10.1016/s0040-4039(00)87634-0  0.383
1982 Hiranuma S, Hudlicky T. Synthesis of homoharringtonine and its derivative . Tetrahedron Letters. 23: 3431-3434. DOI: 10.1016/s0040-4039(00)87634-0  0.383
1982 Hiranuma S, Hudlicky T. Synthesis of homoharringtonine and its derivative . Tetrahedron Letters. 23: 3431-3434. DOI: 10.1016/s0040-4039(00)87634-0  0.383
1982 Hiranuma S, Hudlicky T. Synthesis of homoharringtonine and its derivative . Tetrahedron Letters. 23: 3431-3434. DOI: 10.1016/s0040-4039(00)87634-0  0.383
1981 Hudlicky T, Kutchan TM, Shen G, Sutliff VE, Coscia CJ. Improved synthesis and characterization of Pictet-Spengler adducts of phenylpyruvic acid and biogenic amines Journal of Organic Chemistry. 46: 1738-1741. DOI: 10.1021/Jo00321A047  0.414
1981 Hudlicky T, Srnak T. Aluminum oxide catalyzed isomerization of acylated cycloalkenes Tetrahedron Letters. 22: 3351-3354. DOI: 10.1016/S0040-4039(01)81902-X  0.392
1981 Oppolzer W, Bättig K, Hudlicky T. A total synthesis of (±)-isocomene and (±) β-isocomene by an intramolecular ene reaction Tetrahedron. 37: 4359-4364. DOI: 10.1016/0040-4020(81)80001-4  0.567
1981 HUDLICKY T, KOSZYK FJ, KUTCHAN TM, SHETH JP. ChemInform Abstract: CYCLOPENTENE ANNULATION VIA INTRAMOLECULAR ADDITION OF DIAZOKETONES TO 1,3-DIENES. APPLICATIONS TO THE SYNTHESIS OF CYCLOPENTANOID TERPENES Chemischer Informationsdienst. 12. DOI: 10.1002/chin.198114295  0.378
1980 Hudlicky T, Koszyk FF, Kutchan TM, Sheth JP. Cyclopentene annulation via intramolecular addition of diazoketones to 1,3-dienes. Applications to the synthesis of cyclopentanoid terpenes The Journal of Organic Chemistry. 45: 5020-5027. DOI: 10.1021/Jo01313A003  0.479
1980 Hudlicky T, Koszyk FF, Kutchan TM, Sheth JP. Cyclopentene annulation via intramolecular addition of diazoketones to 1,3-dienes. Applications to the synthesis of cyclopentanoid terpenes The Journal of Organic Chemistry. 45: 5020-5027. DOI: 10.1021/jo01313a003  0.376
1980 Hudlicky T, Koszyk FF, Kutchan TM, Sheth JP. Cyclopentene annulation via intramolecular addition of diazoketones to 1,3-dienes. Applications to the synthesis of cyclopentanoid terpenes The Journal of Organic Chemistry. 45: 5020-5027. DOI: 10.1021/jo01313a003  0.376
1980 Hudlicky T, Koszyk FF, Kutchan TM, Sheth JP. Cyclopentene annulation via intramolecular addition of diazoketones to 1,3-dienes. Applications to the synthesis of cyclopentanoid terpenes The Journal of Organic Chemistry. 45: 5020-5027. DOI: 10.1021/jo01313a003  0.376
1980 Hudlicky T, Koszyk FF, Kutchan TM, Sheth JP. Cyclopentene annulation via intramolecular addition of diazoketones to 1,3-dienes. Applications to the synthesis of cyclopentanoid terpenes The Journal of Organic Chemistry. 45: 5020-5027. DOI: 10.1021/jo01313a003  0.376
1980 Hudlicky T, Koszyk FF, Kutchan TM, Sheth JP. Cyclopentene annulation via intramolecular addition of diazoketones to 1,3-dienes. Applications to the synthesis of cyclopentanoid terpenes The Journal of Organic Chemistry. 45: 5020-5027. DOI: 10.1021/jo01313a003  0.376
1980 Hudlicky T, Koszyk FF, Kutchan TM, Sheth JP. Cyclopentene annulation via intramolecular addition of diazoketones to 1,3-dienes. Applications to the synthesis of cyclopentanoid terpenes The Journal of Organic Chemistry. 45: 5020-5027. DOI: 10.1021/jo01313a003  0.376
1980 Hudlicky T, Koszyk FF, Kutchan TM, Sheth JP. Cyclopentene annulation via intramolecular addition of diazoketones to 1,3-dienes. Applications to the synthesis of cyclopentanoid terpenes The Journal of Organic Chemistry. 45: 5020-5027. DOI: 10.1021/jo01313a003  0.376
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